{"id":680,"date":"2016-12-20T22:00:07","date_gmt":"2016-12-20T22:00:07","guid":{"rendered":"https:\/\/blog.espci.fr\/arseniyadis\/?page_id=10"},"modified":"2026-05-29T02:18:43","modified_gmt":"2026-05-29T01:18:43","slug":"publications","status":"publish","type":"page","link":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/?page_id=680","title":{"rendered":"Publications"},"content":{"rendered":"<div id=\"pl-680\"  class=\"panel-layout\" ><div id=\"pg-680-0\"  class=\"panel-grid panel-no-style\" ><div id=\"pgc-680-0-0\"  class=\"panel-grid-cell\" ><div id=\"panel-680-0-0-0\" class=\"so-panel widget widget_sow-editor panel-first-child panel-last-child\" data-index=\"0\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-sow-editor so-widget-sow-editor-base\"\n\t\t\t\n\t\t>\n<div class=\"siteorigin-widget-tinymce textwidget\">\n\t<p class=\"p1\"><strong>Submitted or in preparation:<\/strong><\/p>\n<p class=\"p1\">[104] Straightforward Access to Diversely Substituted Pyrrolidones via Pd-Catalysed Allylic Substitution of Nitroallyl Derivatives. Mansour Dol\u00e9 Kerim, Stellios Arseniyadis,* Laurent El Kaim* (<em>in preparation<\/em>).<\/p>\n<p class=\"p1\">[103] Stereodivergent iridium-catalyzed asymmetric allylic alkylation of hydantoins. Yao-Rui Ma, Yibing Chen, Paul Clark, Avantika Hasija, Thibaud Bregent, Alexandre Jean, Pei\u2011Qiang Huang,* Guillaume Lef\u00e8vre,* Stellios Arseniyadis* (<em>in preparation<\/em>).<\/p>\n<p>[102] Collective asymmetric synthesis and structure elucidation of the butenolide-containing monoterpenoids capnolactone, excavatin K, clauslactone K, anisolactone, indicolactone and tuberatolide A. Thomas Keenan, Fran\u00e7ois Richard, Paul Clark, Phinyada Kankraisri, Sidonie Aubert, Thibaud Bregent, Alexandre Jean,<sup>\u00a0<\/sup>Andrei Corbu,* and Stellios Arseniyadis*\u00a0<span lang=\"EN-US\">(<em>in preparation<\/em>).<\/span><\/p>\n<p class=\"p1\">[101] Site-selective aryne-mediated <em>N<\/em>-arylation of polypetides. Phinyada Kankraisri, Khushal Siddiq,<span class=\"s1\">\u00a0<\/span>Yao-Rui Ma,<span class=\"s1\">\u00a0<\/span>Jonathan Beadle,<span class=\"s1\">\u00a0<\/span>Stephen Gregson,<span class=\"s1\">\u00a0<\/span>Luke Masterson,<span class=\"s1\">\u00a0<\/span>Christina Von Bulow,<span class=\"s1\">\u00a0<\/span>Pei-Qiang Huang,<span class=\"s1\">\u00a0<\/span>Stellios Arseniyadis* Christopher R. Jones* (<em>submitted<\/em>)<i>.<\/i><\/p>\n<p class=\"p1\">[100] A bioactive radiopaque infiltrant for managing early enamel carious lesions. Mahmoud Abdelgawad Hasan, Amina Khatoon, Stellios Arseniyadis, Mangala Patel, Robert Hill, Ferranti S. L. Wong (<em>submitted<\/em>).<\/p>\n<p class=\"p1\">[99] Positional nitrogen insertion for tuning optoelectronic properties of double helicenes and Dibenzo-Terrylenes. Vikas Sharma, Kaicheng Zhang, David Preston, Doppalapudi Vineet Kumar, George F. S. Whitehead, Louise Natrajan, Shane R. Dunne,<span class=\"s1\">\u00a0<\/span>Basker Sundararaju, Stellios Arseniyadis<span class=\"s1\">,<\/span>* Ashok Keerthi<span class=\"s1\">* (<i>under revision<\/i><\/span>).<\/p>\n<p><strong><span lang=\"EN-US\">In press:<\/span><\/strong><\/p>\n<p><span lang=\"EN-US\">[98] <a href=\"https:\/\/doi.org\/10.1021\/jacsau.6c00334\">Catalyst-controlled Regiodivergent C\u2013H Olefination of Furanyl Carbamates through a Rational Approach.<\/a> Francois Richard, Morgan Languet, Cora Escande de Messi\u00e8res, Alexandre Dupas, Ahmed M. Zaitoun, Xacobe Cambeiro, Janine Cossy,* Stellios Arseniyadis* <em>JACS Au<\/em>\u00a0<strong>2026<\/strong> (<em>in press<\/em>).<\/span><\/p>\n<p><span lang=\"EN-US\">[97] <a href=\"https:\/\/www.nature.com\/articles\/s41467-026-72881-z\">A metal-DNA biohybrid as enantioselective artificial PhotoDNAzyme<\/a>. Zachary Pastorel, Juliette Zanzi, Alessio Bartocci, Stellios Arseniyadis, Elise Dumont, Yves Canac,* Olivier Basl\u00e9,* Michael Smietana* <em>Nat. Commun.<\/em> <strong>2026 <\/strong>(<em>in press<\/em>).\u00a0<\/span><\/p>\n<p>[96] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202521362\">Late-stage oxidation in organic synthesis: From innate reactivity to guided selectivity in complex settings<\/a>. Kyriaki Gennaiou, Maria Kourgiantaki, Kalliopi Mazaraki, Fran\u00e7ois Richard, Nicolas Fincias, Stellios Arseniyadis,* Alexandros L. Zografos*<em><span lang=\"EN-US\"> Angew. Chem. Int. Ed<\/span><\/em><span lang=\"EN-US\">. <strong>2026<\/strong>, <em>65<\/em>, e21362.<\/span><\/p>\n<p><span lang=\"EN-US\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-2865 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/TOC.png\" alt=\"\" width=\"335\" height=\"287\" \/><\/span><\/p>\n<p>[95] <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2026\/cc\/d6cc01851c\">Bioinspired Total Synthesis of (Dibromo)Sceptrin and (Dibromo)Ageliferin.<\/a> Mohammed Latrache, Amina Sesay, Samuel Oger, Mireia Benito Montaner, Mohamed Mellah, Erwan Poupon, Stephen T. Hilton, Stellios Arseniyadis, Laurent Evanno* <span lang=\"EN-US\"><em>Chem. Commun.<\/em> <strong>2026<\/strong> (<em>in press<\/em>).<\/span><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2863 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/Image1-300x166.jpg\" alt=\"\" width=\"412\" height=\"228\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/Image1-300x166.jpg 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/Image1-1024x566.jpg 1024w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/Image1-768x424.jpg 768w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/Image1-1536x849.jpg 1536w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/Image1-2048x1131.jpg 2048w\" sizes=\"auto, (max-width: 412px) 100vw, 412px\" \/><\/p>\n<p class=\"BATitle\" style=\"text-align: left;\"><span lang=\"EN-US\">[94] <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2026\/cc\/d6cc01304j\">Unified, Catalyst-Controlled, Bioinspired Total Synthesis of Dimeric Piperine Alkaloids in Batch and Flow<\/a><\/span>. <span lang=\"EN-US\">Mohammed Latrache, Amina Sesay, Samuel Oger, Mireia Benito Montaner, Jinlei Zhang, Mohamed Mellah, Erwan Poupon, Stephen T. Hilton, Stellios Arseniyadis, Laurent Evanno* <em>Chem. Commun.<\/em> <strong>2026<\/strong> (<em>in press<\/em>).<\/span><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/TOC-sceptrin.pdf\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2026\/05\/Untitled-scaled.jpg\" width=\"412\" height=\"206\" \/><\/a>[93] <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/cc\/d5cc05328e\">Palladium-catalysed asymmetric allylic alkylation of hydantoins using bench-stable chiral palladium precatalysts<\/a>. <span lang=\"EN-US\">Paul Clark, Thomas Keenan, Shiqi Liu, Jingjun Huang,<span class=\"article__author-link\"> Yao-Rui Ma, <\/span><span class=\"article__author-link\">Avantika Hasija, Pei-Qiang Huang, <\/span>Alexandre Jean, David C. Leitch,* Stellios Arseniyadis* <em>Chem. Commun<\/em>. <strong>2025<\/strong>, <em>61, <\/em>19064<span class=\"cit-pageRange\">\u2013<\/span>19067.<\/span><\/p>\n<p class=\"BATitle\" style=\"text-align: left;\"><span lang=\"EN-US\">[92] <\/span><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2026\/cc\/d6cc00637j\">Copper-catalyzed allylic substitution of nitroally derivatives with Grignard reagents.<\/a> <span lang=\"EN-US\">Louis Clavier, Nicolas Fincias, Stellios Arseniyadis,* Laurent El Kaim* <em>Chem. Commun.<\/em> <strong>2026<\/strong>, <em>62<\/em>, 6950<span class=\"cit-pageRange\">\u2013<\/span>6953.<\/span><\/p>\n<p><span lang=\"EN-US\">[91] <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0300571225004397\"><span data-olk-copy-source=\"MessageBody\">A novel radiopaque resin infiltrant for managing early enamel caries<\/span>.<\/a> Mahmoud Mohammed Hasan, Amina Khatoon, Stellios Arseniyadis, Mangala Patel, Ferranti S. L. Wong* <em>J. Dent.<\/em> <strong>2025<\/strong>, <em>161<\/em>, 105995.<\/span><\/p>\n<p><span lang=\"EN-US\">[90] <a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/jacsau.4c00809\">Unlocking copper catalysis with nitro compounds: Synthesis of functionalized allylboranes from allylic nitroalkanes<\/a>. Nicolas Fincias, Louis Clavier, Cora Escande de Messi\u00e8res,<sup>\u00a0<\/sup>Marianne Guillard, Mansour Dole Kerim, Nicolas Casaretto, Julian Garrec, Stellios Arseniyadis,* Laurent El Ka\u00efm* <em>JACS Au<\/em> <strong>2025<\/strong>, <em><span class=\"cit-volume\">5<\/span><\/em><span class=\"cit-issue\">,<\/span><span class=\"cit-pageRange\"> 99\u2013110<\/span>.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2714\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-1024x338.jpg\" alt=\"\" width=\"540\" height=\"178\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-1024x338.jpg 1024w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-300x99.jpg 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-768x253.jpg 768w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-1536x506.jpg 1536w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-2048x675.jpg 2048w\" sizes=\"auto, (max-width: 540px) 100vw, 540px\" \/><\/p>\n<p>[89] <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlepdf\/2024\/cc\/d4cc02557a?page=search\">Visible light-mediated difluoromethylation\/cyclization in batch and flow: Scalable synthesis of CHF<sub>2<\/sub>-containing benzimidazo- and indolo[2,1-<em>a<\/em>]isoquinolin-6(5<em>H<\/em>)-ones.<\/a> Al Hannam, Phinyada Kankraisri, Karan R. Thombare, Prahallad Meher, Alexandre Jean, Stephen T. Hilton, Sandip Murarka,* Stellios Arseniyadis* <em>Chem. Commun<\/em>. <strong>2024<\/strong>, <span lang=\"EN-US\"><em>60<\/em>, 7938-7941.<\/span><\/p>\n<p>[88] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.3c03997\">Synthesis of CHF<sub>2<\/sub>-containing heterocycles through oxy-difluoromethylation using low-cost 3D-printed photoflow reactors.<\/a> Jinlei Zhang, Elias Selmi-Higashi, Shen Zhang, Alexandre Jean, Stephen T. Hilton,* Xacobe C. Cambeiro,* Stellios Arseniyadis* <em>Org. Lett.<\/em> <strong>2024<\/strong>, <em><span class=\"cit-volume\">26<\/span><\/em><span class=\"cit-pageRange\">, 2877\u20132882<\/span><span lang=\"EN-US\">.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2698 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/01\/Picture-1-1-300x100.png\" alt=\"\" width=\"551\" height=\"183\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/01\/Picture-1-1-300x100.png 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/01\/Picture-1-1.png 452w\" sizes=\"auto, (max-width: 551px) 100vw, 551px\" \/><\/p>\n<p><span lang=\"EN-US\">[87] <\/span><a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2024\/CS\/D3CS00856H\">Pd-Catalysed Asymmetric Allylic Alkylation of Heterocycles: A User\u2019s Guide.<\/a> Fran\u00e7ois Richard, Paul Clark, Al Hannam, Thomas Keenan, Alexandre Jean, Stellios Arseniyadis* <em>Chem. Soc. Rev.<\/em> <strong>2024<\/strong>, <em>53<\/em>, 1936<span lang=\"EN-US\"><span class=\"cit-pageRange\">\u2013<\/span><\/span>1983.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-2690 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/01\/Picture-1-300x181.png\" alt=\"\" width=\"406\" height=\"245\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/01\/Picture-1-300x181.png 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/01\/Picture-1.png 407w\" sizes=\"auto, (max-width: 406px) 100vw, 406px\" \/><\/p>\n<p>[86] <a href=\"https:\/\/www.nature.com\/articles\/s41467-023-43512-8\">Chiral, air stable, and reliable Pd(0) precatalysts applicable to asymmetric allylic alkylation chemistry<\/a><span lang=\"EN-US\">. Jingjun Huang, Thomas Keenan, Francois Richard,<span style=\"font-size: small;\">\u00a0<\/span>Jingru Lu,<span style=\"font-size: small;\">\u00a0<\/span>Sarah E. Jenny,<span style=\"font-size: small;\">\u00a0<\/span>Alexandre Jean,<span style=\"font-size: small;\">\u00a0<\/span>Stellios Arseniyadis,* David C. Leitch* <em>Nat. Commun.<\/em> <strong>2023<\/strong>, <em>14<\/em>, 8058. Highlighted in <a href=\"https:\/\/d-nb.info\/132523365X\/34\"><em>Synform<\/em><\/a> and <a href=\"https:\/\/pubs.acs.org\/doi\/epdf\/10.1021\/acs.oprd.4c00036\"><em>OPRD<\/em><\/a>.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2718 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Picture-2-1-300x209.png\" alt=\"\" width=\"549\" height=\"382\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Picture-2-1-300x209.png 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Picture-2-1.png 581w\" sizes=\"auto, (max-width: 549px) 100vw, 549px\" \/><\/p>\n<p class=\"BATitle\" style=\"text-align: left;\"><span lang=\"EN-US\">[85] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/9781119774167.ch18\">Late-stage functionalisation of pharmaceuticals, agrochemicals and natural products<\/a>. Fran\u00e7ois Richard, Elias Selmi-Higashi, Stellios Arseniyadis in Transition-metal-catalyzed C-H functionalization of heterocycles (Ed. T. Punniyamurthy and A. Kumar), Wiley &amp; Sons <strong>2023<\/strong>, chapter 18.<\/span><\/p>\n<p class=\"BATitle\" style=\"text-align: left;\"><span lang=\"EN-US\">[84] <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2023\/cc\/d3cc00673e\">Expanding the 'aplysinospin cascade' through DNA-templated [2+2] photocycloaddition<\/a>.\u00a0Samuel Oger, Nicolas Duchemin,<span style=\"font-size: small;\">\u00a0<\/span>Mayssa Bendiab,<span style=\"font-size: small;\">\u00a0<\/span>Nicolas Birlirakis,<span style=\"font-size: small;\">\u00a0<\/span>Adam Skiredj,<span style=\"font-size: small;\">\u00a0<\/span>Somia\u00a0Rharrabti,<span style=\"font-size: small;\">\u00a0<\/span>Remi Franco,<span style=\"font-size: small;\">\u00a0<\/span>Erwan Poupon,* Michael Smietana,* Stellios Arseniyadis,* Laurent Evanno* <em>Chem. Commun.\u00a0<\/em><strong>2023<\/strong>,<i> 59<\/i>, 4221<span class=\"cit-pageRange\">\u20134224<\/span>.<\/span><\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2636\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2023\/03\/Sans-titre-300x152.png\" alt=\"\" width=\"440\" height=\"222\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2023\/03\/Sans-titre-300x152.png 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2023\/03\/Sans-titre.png 530w\" sizes=\"auto, (max-width: 440px) 100vw, 440px\" \/><\/p>\n<p style=\"text-align: left;\">[83] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacsau.2c00271\"><span lang=\"EN-US\">A new benchmark in DNA-based asymmetric catalysis: Prevalence of modified DNA\/RNA hybrid systems<\/span><\/a>. Nicolas Duchemin,<sup>\u00a0<\/sup>Sidonie Aubert, Jo\u00e3o V. de Souza, Lucas Bethge, <span lang=\"EN-US\">Stefan\u00a0Vonhoff,\u00a0<\/span>Agnieszka K. Bronowska, Michael Smietana,* Stellios Arseniyadis* <em>JACS Au<\/em> <strong>2022<\/strong>,\u00a0<span class=\"cit-volume\">2<\/span><span class=\"cit-issue\">, <\/span><span class=\"cit-pageRange\">1910\u20131917<\/span>. <img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2603 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/07\/Abstract-JACS-Au-300x98.png\" alt=\"\" width=\"623\" height=\"203\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/07\/Abstract-JACS-Au-300x98.png 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/07\/Abstract-JACS-Au-768x250.png 768w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/07\/Abstract-JACS-Au.png 896w\" sizes=\"auto, (max-width: 623px) 100vw, 623px\" \/><\/p>\n<p style=\"text-align: left;\"><img class=\"aligncenter\" \/><\/p>\n<p style=\"text-align: left;\">[82] <a href=\"https:\/\/www.nature.com\/articles\/s44160-022-00109-1\">Enantioselective synthesis of \u03b3-butenolides through Pd-catalysed\u00a0C5-selective allylation of siloxyfurans.<\/a>\u00a0Fran\u00e7ois Richard,<span style=\"font-size: small;\">\u00a0<\/span>Sidonie Aubert,<span style=\"font-size: small;\">\u00a0<\/span>Tania Katsina,<span style=\"font-size: small;\">\u00a0<\/span>Luuk Reinalda,<span style=\"font-size: small;\">\u00a0<\/span>David Palomas,<span style=\"font-size: small;\">\u00a0<\/span>Rachel\u00a0Crespo-Otero,<span style=\"font-size: small;\">\u00a0<\/span>Jingjun Huang,<span style=\"font-size: small;\">\u00a0<\/span>David C. Leitch,<span style=\"font-size: small;\">\u00a0<\/span>Carlos Mateos,<span style=\"font-size: small;\">\u00a0<\/span>Stellios Arseniyadis* <em>Nat. Synth.<\/em>\u00a0<strong>2022<\/strong>, <em>1<\/em>, 641\u2013648.<\/p>\n<ul>\n<li><a href=\"https:\/\/www.nature.com\/articles\/s44160-022-00111-7\">Research Briefing<\/a>.<\/li>\n<\/ul>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2602\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/07\/Abstract-Nat-Synth-300x105.png\" alt=\"\" width=\"577\" height=\"203\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/07\/Abstract-Nat-Synth-300x105.png 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/07\/Abstract-Nat-Synth-768x270.png 768w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/07\/Abstract-Nat-Synth.png 879w\" sizes=\"auto, (max-width: 577px) 100vw, 577px\" \/><\/p>\n<p style=\"text-align: left;\"><img class=\"aligncenter\" \/><\/p>\n<p class=\"BATitle\" style=\"text-align: left;\"><span lang=\"EN-US\">[81]<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsorginorgau.1c00058\"> Phase-transfer catalyzed alkylation of hydantoins.<\/a>\u00a0<\/span><span lang=\"EN-US\">Thomas Keenan,<span style=\"font-size: small;\">\u00a0<\/span>Alexandre Jean,*<span style=\"font-size: small;\">\u00a0<\/span>Stellios Arseniyadis* <em>ACS Organic &amp; Inorganic Au<\/em>\u00a0<strong>2022<\/strong><span class=\"cit-volume\">, 2<\/span><span class=\"cit-issue\">,<\/span><span class=\"cit-pageRange\">\u00a0<\/span><span class=\"cit-pageRange\">312<\/span><span class=\"cit-pageRange\">\u2013<\/span><span class=\"cit-pageRange\">317<\/span>.<\/span><\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2517\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/02\/gg1c00058_0007-300x140.jpeg\" alt=\"\" width=\"397\" height=\"186\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/02\/gg1c00058_0007-300x140.jpeg 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/02\/gg1c00058_0007-1024x480.jpeg 1024w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/02\/gg1c00058_0007-768x360.jpeg 768w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2022\/02\/gg1c00058_0007.jpeg 1168w\" sizes=\"auto, (max-width: 397px) 100vw, 397px\" \/><\/p>\n<p style=\"text-align: left;\">[80] <a href=\"https:\/\/www.worldscientific.com\/doi\/abs\/10.1142\/9789811248436_0001\">DNA-based asymmetric catalysis: Past, present and future<\/a>. Sidonie Aubert, Nicolas Duchemin, Jin-Lei Zhang, Michael Smietana, Stellios Arseniyadis* in Enantioselective Catalysis, Book series: Series on Chemistry, Energy and the Environment (Ed. A. Marinetti), World Scientific <strong>2022<\/strong> (<em>DOI: 10.1142\/9789811248436_0001<\/em>).<\/p>\n<p style=\"text-align: left;\">[79] <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/B9780128186558001591\">Four-membered rings with one sulfur and one nitrogen atom<\/a>.\u00a0Fran\u00e7ois Richard, Jennifer Ciesielski, Stellios\u00a0Arseniyadis in\u00a0<em>Comprehensive Heterocyclic Chemistry IV<\/em>, (Ed. G. Evano), Elsevier <strong>2021<\/strong> (<em>in press<\/em>).<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-2508 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2021\/12\/9780128186558.jpeg\" alt=\"\" width=\"198\" height=\"259\" \/><\/p>\n<p style=\"text-align: left;\">[78] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.1c01177\"><span lang=\"EN-US\">Synthesis of \u03b1<\/span><span lang=\"EN-US\">-difluoromethyl aryl ketones through a photoredox difluoromethylation of enol silanes<\/span>.<\/a> <span lang=\"EN-US\">Elias Selmi-Higashi, Jinlei Zhang,<\/span> Xacobe C. Cambeiro, Stellios Arseniyadis* <em>Org. Lett<\/em>. <strong>2021<\/strong>, 23, 4239<span class=\"cit-pageRange\">\u2013<\/span>4243.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2479\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2021\/04\/TOC.png\" alt=\"\" width=\"437\" height=\"203\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2021\/04\/TOC.png 462w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2021\/04\/TOC-300x140.png 300w\" sizes=\"auto, (max-width: 437px) 100vw, 437px\" \/><\/p>\n<p style=\"text-align: left;\">[77] <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0040-1706019\"><span class=\"Style1Char\">4-Cyano-3-oxotetrahydrothiophene (c-THT): An ideal acrylonitrile anion equivalent<\/span><\/a>.\u00a0Fran\u00e7ois Richard, Carlos Mateos, Stellios\u00a0Arseniyadis* <em>SynOpen<\/em> <strong>2021, <\/strong><em>5<\/em>, 25\u201328.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2480 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2021\/04\/Sans-titre-300x126.png\" alt=\"\" width=\"397\" height=\"167\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2021\/04\/Sans-titre-300x126.png 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2021\/04\/Sans-titre-768x322.png 768w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2021\/04\/Sans-titre.png 811w\" sizes=\"auto, (max-width: 397px) 100vw, 397px\" \/><\/p>\n<p style=\"text-align: left;\">[76] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.0c01721\"><em>O<\/em>-Allylated Pudovik and Passerini adducts as versatile templates for product diversification<\/a>.\u00a0Mansour Dol\u00e9 Kerim,\u00a0Tania Katsina,\u00a0Martin Cattoen,\u00a0Nicolas Fincias,\u00a0Stellios Arseniyadis,*\u00a0Laurent El Ka\u00efm* <em>J. Org. Chem<\/em>. <strong>2020<\/strong>,\u00a0<em><span class=\"cit-volume\">85<\/span><\/em><span class=\"cit-pageRange\">, 12514\u201312525<\/span>.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2440\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2020\/09\/TOC-75.png\" alt=\"\" width=\"450\" height=\"173\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2020\/09\/TOC-75.png 502w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2020\/09\/TOC-75-300x115.png 300w\" sizes=\"auto, (max-width: 450px) 100vw, 450px\" \/><\/p>\n<p style=\"text-align: left;\">[75] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c02079\">Direct access to highly enantioenriched \u03b1-branched acrylonitriles through a one-pot sequential asymmetric Michael addition\/retro-Dieckmann\/retro-Michael fragmentation cascade.<\/a> Nicolas Duchemin, Martin Cattoen, Oscar Gayraud, Silvia Anselmi, Bilal Siddiq, Roberto Buccafusca,\u00a0Marc Daumas, Vincent Ferey, Michael Smietana, Stellios Arseniyadis* <em>Org. Lett.<\/em> <strong>2020<\/strong>, <span class=\"cit-volume\">22<\/span><span class=\"cit-issue\">,<\/span><span class=\"cit-pageRange\"> 5995-6000.<\/span><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2367\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2020\/04\/TOC.png\" alt=\"\" width=\"550\" height=\"203\" \/><\/p>\n<p style=\"text-align: left;\">[74] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.9b00513\">Aerobic oxidation of alcohols using catalytic DDQ\/HNO3<\/a>.\u00a0Tania Katsina,\u00a0Louis Clavier,\u00a0Jean-Fran\u00e7ois Giffard,\u00a0Nayane Macedo Portela da Silva,\u00a0Jean Fournier<b>,<\/b><b>\u00a0<\/b>Chlo\u00e9 Copin,<b>\u00a0<\/b>Stellios Arseniyadis,*\u00a0Alexandre Jean* <span class=\"cit-title\"><i>Org. Process Res. Dev.<\/i><\/span> <span class=\"cit-year-info\"><strong>2020<\/strong><\/span>, <span class=\"cit-volume\">24<\/span><span class=\"cit-issue\">,<\/span><span class=\"cit-pageRange\">\u00a0856-860<\/span>.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2351\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2020\/03\/op9b00513_0005.jpeg\" alt=\"\" width=\"473\" height=\"143\" \/><\/p>\n<p style=\"text-align: left;\">[73] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/chem.202000516\">DNA-based asymmetric inverse electron-demand hetero-Diels-Alder<\/a>. Justine Mansot, Jimmy Lauberteaux, Aur\u00e9lien Lebrun, Marc Mauduit, Jean-Jacques Vasseur, Renata Marcia de Figueiredo, Stellios Arseniyadis,* Jean-Marc Campagne,* Michael Smietana*\u00a0<em>Chem. Eur. J<\/em>. <strong>2020<\/strong>, <em>26<\/em>, 3519<span class=\"cit-pageRange\">\u2013<\/span>3523.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-2329\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2020\/02\/Capture-d\u2019\u00e9cran-2020-02-03-\u00e0-12.49.04.png\" alt=\"\" width=\"542\" height=\"140\" \/><\/p>\n<p style=\"text-align: left;\">[72] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b03522\">A Sequential palladium\u2011catalyzed allylic alkylation\/retro-Dieckmann fragmentation strategy for the synthesis of \u03b1-substituted acrylonitriles<\/a>.\u00a0Tania Katsina,\u00a0Sachi Sharma,\u00a0Roberto Buccafusca,\u00a0Derek J. Quinn,\u00a0Thomas S. Moody,\u00a0Stellios Arseniyadis* <em>Org. Lett<\/em>.\u00a0<strong>2019<\/strong><i>,\u00a0<\/i><em><span class=\"cit-volume\">21<\/span><\/em><span class=\"cit-issue\">, <\/span><span class=\"cit-pageRange\">9348\u20139352<\/span>.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2234 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2019\/11\/ol9b03522_0009.jpg\" alt=\"\" width=\"442\" height=\"134\" \/><\/p>\n<p style=\"text-align: left;\">[71] <a href=\"https:\/\/www.nature.com\/articles\/s41570-019-0139-6#Abs1\">Spatial and temporal control of chemical processes.<\/a>\u00a0Sidonie Aubert,\u00a0Marine Bezagu,\u00a0Alan C. Spivey,*\u00a0Stellios Arseniyadis* <em>Nature Rev. Chem.<\/em>\u00a0<strong>2019<\/strong>,\u00a0<em><b data-test=\"journal-volume\">3<\/b><\/em>,\u00a0706\u2013722.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-2311 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2020\/01\/Capture-d\u2019\u00e9cran-2020-01-31-\u00e0-19.17.46.png\" alt=\"\" width=\"466\" height=\"196\" \/><\/p>\n<p style=\"text-align: left;\">[70] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b02887\">A unified strategy for the synthesis of difluoromethyl- and vinylfluoride-containing scaffolds<\/a>. Nicolas Duchemin, Roberto Buccafusca, Marc Daumas, Vincent Ferey, Stellios Arseniyadis*\u00a0<em>Org. Lett.<\/em>\u00a0<strong>2019<\/strong>, 21, 8205<span class=\"cit-pageRange\">\u2013<\/span>8210. Highlighted in <a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.oprd.9b00465\">OPR&amp;D<\/a>.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-1965 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2019\/05\/Abstract-CHF2-1-.png\" alt=\"\" width=\"533\" height=\"284\" \/><\/p>\n<p style=\"text-align: left;\">[69] <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/sc\/c8sc05543b#!divAbstract\">A rational quest for selectivity through precise ligand-positioning in the tandem DNA-catalysed Friedel-Crafts alkylation\/asymmetric protonation<\/a>. Justine Mansot, Sidonie Aubert,\u00a0Nicolas Duchemin,\u00a0Jean-Jacques Vasseur, Stellios Arseniyadis,* Michael Smietana* <em>Chem. Sci<\/em>. <strong>2019, <\/strong>10, 2875<span class=\"cit-pageRange\">\u2013<\/span>2881.<img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1855 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2019\/01\/TOC-reprot-.png\" alt=\"\" width=\"581\" height=\"193\" \/><\/p>\n<p style=\"text-align: left;\">[68] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b00521\">A sequential Pd-AAA\/CM\/Cope rearrangement strategy for the stereoselective synthesis of \u03b3-butenolides.<\/a>\u00a0Sidonie Aubert,\u00a0Tania Katsina,\u00a0Stellios Arseniyadis* <em>Org. Lett<\/em>. <strong>2019<\/strong>, 21 , 2231<span class=\"cit-pageRange\">\u2013<\/span>2235.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-1917\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2019\/03\/Abstract-OL-19.png\" alt=\"\" width=\"570\" height=\"134\" \/><\/p>\n<p style=\"text-align: left;\">[67] <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.8b03613\">Asymmetric synthesis of \u03b1-quaternary \u03b3-lactams through palladium-catalyzed asymmetric allylic alkylation<\/a>. Tao Song, Stellios Arseniyadis,* Janine Cossy* <em>Org. Lett<\/em>. <strong>2019<\/strong>, 21, 603<span class=\"cit-pageRange\">\u2013<\/span>607.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-1839 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2019\/01\/ol-2018-03613k_0010-1.gif\" alt=\"\" width=\"500\" height=\"154\" \/><\/p>\n<p style=\"text-align: left;\">[66] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cctc.201900743\">\u03b1,\u03b2-Unsaturated 2-acyl-imidazoles in asymmetric biohybrid catalysis.<\/a>\u00a0Justine Mansot,\u00a0Jean-Jacques Vasseur,\u00a0Stellios Arseniyadis,* Michael Smietana* <em>ChemCatChem.<\/em> <strong>2019,\u00a0<\/strong><em>11<\/em>, 5686\u20135704.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1966 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2019\/05\/Chem-chat-chem-TOC.png\" alt=\"\" width=\"498\" height=\"108\" \/><\/p>\n<p style=\"text-align: left;\">[65] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.201806357\">DNA-templated [2+2] photocycloaddition: A straightforward entry into the aplysinopsin family of natural products.<\/a> Nicolas Duchemin,\u00a0Adam Skiredj,\u00a0Justine Mansot, Karine Leblanc, Jean-Jacques Vasseur, Mehdi A. Beniddir, Laurent Evanno,* Erwan Poupon,* Michael Smietana,* Stellios Arseniyadis*\u00a0<em>Angew. Chem. Int. Ed.<\/em><em>\u00a0<\/em><strong>2018<\/strong>, <em>57<\/em>, 11786<span class=\"cit-pageRange\">\u2013<\/span>11791. Highlighted in <a href=\"https:\/\/www.nature.com\/articles\/s41570-018-0028-4\"><em>Nature Reviews Chemistry<\/em><\/a>\u00a0and in the <a href=\"http:\/\/www.cnrs.fr\/inc\/communication\/direct_labos\/poupon.htm\">CNRS website<\/a>.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1581 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2018\/07\/abstract-DNA.png\" alt=\"\" width=\"415\" height=\"189\" \/><\/p>\n<p style=\"text-align: left;\">[64] <a href=\"http:\/\/www.ingentaconnect.com\/content\/scs\/chimia\/2018\/00000072\/00000009\/art00011;jsessionid=66g42krskfs47.x-ic-live-03\">Challenges and opportunities in DNA-based asymmetric catalysis<\/a>. Michael Smietana,*\u00a0Stellios Arseniyadis*\u00a0<em>Chimia<\/em><em>\u00a0<\/em><strong>2018<\/strong>, <em>72<\/em>,\u00a0<i>630<span class=\"cit-pageRange\">\u2013<\/span>634 - invited article<\/i>.<\/p>\n<p style=\"text-align: left;\">[63] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/chem.201800920\">Highly enantioselective, base-free synthesis of \u03b1-quaternary\u00a0succinimides through catalytic asymmetric allylic alkylation<\/a>.<em>\u00a0<\/em>Tao Song, Stellios Arseniyadis,* Janine Cossy* <em>Chem. Eur. J.<\/em>\u00a0<strong>2018<\/strong>, <em>24<\/em>, 8076<span class=\"cit-pageRange\">\u2013<\/span>8080 (selected as a <em>Hot Paper<\/em>).\u00a0Highlighted in<em>\u00a0<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/pdf\/10.1055\/s-0037-1610493.pdf?update=true\">Synfact<\/a>.<\/em><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1338 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2018\/07\/Abs-ChemEurJ-Tao.png\" alt=\"\" width=\"550\" height=\"120\" \/><\/p>\n<p style=\"text-align: left;\">[62] <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201800641\/full\">Palladium-catalyzed asymmetric allylic alkylation of 4-substituted isoxazolidin-5-ones: A straightforward access to <\/a><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cctc.201900743\">\u03b2<\/a><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201800641\/full\"><sup>2,2<\/sup>\u2011amino acids<\/a>.<em>\u00a0<\/em>Marllon Nascimento de Oliveira, Stellios Arseniyadis,* Janine Cossy*\u00a0<em>Chem. Eur. J.\u00a0<\/em><strong>2018<\/strong>,\u00a0<em><span class=\"ff8 current-selection\">24<\/span><\/em><span class=\"ls48\"><span class=\"current-selection\">, 4<\/span><span class=\"ls0\"><span class=\"current-selection\">810<span class=\"cit-pageRange\">\u2013<\/span><\/span><span class=\"ls49\"><span class=\"current-selection\">4<\/span><span class=\"ls0 current-selection\">814<\/span><\/span><\/span><\/span>.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1257 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2018\/07\/Abs-ChemEurJ2018-Marllon.png\" alt=\"\" width=\"550\" height=\"96\" \/><\/p>\n<p style=\"text-align: left;\">[61] <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.201701150\/abstract?systemMessage=Wiley+Online+Library+usage+report+download+page+will+be+unavailable+on+Friday+24th+November+2017+at+21%3A00+EST+%2F+02.00+GMT+%2F+10%3A00+SGT+%28Saturday+25th+Nov+for+SGT+\">Palladium-catalysed <em>O<\/em>-allylation of <\/a><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.8b03613\">\u03b1<\/a><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.201701150\/abstract?systemMessage=Wiley+Online+Library+usage+report+download+page+will+be+unavailable+on+Friday+24th+November+2017+at+21%3A00+EST+%2F+02.00+GMT+%2F+10%3A00+SGT+%28Saturday+25th+Nov+for+SGT+\">-hydroxyphosphonates: An\u00a0expedient entry into phosphono-oxaheterocycles<\/a>.\u00a0Mansour Dol\u00e9 Kerim,\u00a0Martin Cattoen,\u00a0Nicolas Fincias,\u00a0Aur\u00e9lie Dos Santos,\u00a0Stellios Arseniyadis,* Laurent El Ka\u00efm* <em>Adv. Synth. &amp; Catal<\/em>. <strong>2018<\/strong>,\u00a0<em><span class=\"current-selection\">360<\/span><\/em><span class=\"ff6\"><span class=\"current-selection\">,<\/span> <span class=\"current-selection\">449<span class=\"cit-pageRange\">\u2013<\/span><\/span><span class=\"current-selection\">454 (selected as a\u00a0<em>Very Important Publication<\/em>)<\/span><\/span>.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1254 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2018\/07\/AbstractASC.jpg\" alt=\"\" width=\"550\" height=\"176\" \/><\/p>\n<p style=\"text-align: left;\">[60] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/9781118940228.ch6\">Recent applications of Kagan's reagent (SmI2) in natural product synthesis<\/a>. Erica Benedetti, Cyril Bressy, Michael Smietana, Stellios\u00a0Arseniyadis in\u00a0<em>Efficiency in Natural Products Total Synthesis<\/em>, (Eds. P.-Q. Huang, Z.-J. Yao, R.\u00a0P.\u00a0Hsung), Wiley <strong>2018<\/strong>, ch 8, 319<span class=\"cit-pageRange\">\u2013<\/span>344.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" id=\"imgBlkFront\" class=\"a-dynamic-image aligncenter\" src=\"https:\/\/images-na.ssl-images-amazon.com\/images\/I\/51SKs0u2vvL._SX330_BO1,204,203,200_.jpg\" alt=\"\" width=\"259\" height=\"389\" data-a-dynamic-image=\"{&quot;https:\/\/images-na.ssl-images-amazon.com\/images\/I\/51SKs0u2vvL._SY344_BO1,204,203,200_.jpg&quot;:[230,346],&quot;https:\/\/images-na.ssl-images-amazon.com\/images\/I\/51SKs0u2vvL._SX330_BO1,204,203,200_.jpg&quot;:[332,499]}\" \/><\/p>\n<p style=\"text-align: left;\">[59] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/9781118940228.ch8\">Multicomponent reactions in\u00a0natural product\u00a0synthesis<\/a>. Michael Smietana, Erica Benedetti, Cyril Bressy, Stellios\u00a0Arseniyadis in\u00a0<em>Efficiency in Natural Products Total Synthesis<\/em>, (Eds. P.-Q. Huang, Z.-J. Yao, R.\u00a0P.\u00a0Hsung), Wiley <strong>2018,\u00a0<\/strong>ch 6, 273<span class=\"cit-pageRange\">\u2013<\/span>295.<\/p>\n<p style=\"text-align: left;\">[58] <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2018\/dt\/c8dt00538a#!divAbstract\">Dinucleating Schiff base ligand in Zn\/4f coordination chemistry: Synthetic challenges and catalytic activity evaluation.<\/a> Stavroula I. Sampani,\u00a0Sidonie Aubert,\u00a0Martin Cattoen,\u00a0Kieran Griffiths,\u00a0Alaa Abdul-Sada,\u00a0Geoffrey R. Akien,\u00a0Graham J. Tizzard,\u00a0Simon J. Coles,\u00a0Stellios Arseniyadis,* George\u00a0E.\u00a0Kostakis*\u00a0<em>Dalton Trans.<\/em> <strong>2018, <\/strong><em>47<\/em>, 4486<span class=\"cit-pageRange\">\u2013<\/span>4493.<img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1261 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2018\/07\/Abs-Dalton-2018-Georges-1.png\" alt=\"\" width=\"597\" height=\"155\" \/><\/p>\n<p style=\"text-align: left;\">[57] <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/ob\/c7ob00176b#!divAbstract\">A decade of DNA-hybrid catalysis: from innovation to comprehension<\/a>. Nicolas Duchemin, Isabelle Heath-Apostolopoulos,\u00a0Michael Smietana,*\u00a0Stellios Arseniyadis*\u00a0<em>Org. Biomol. Chem<\/em>.<em>\u00a0<\/em><strong>2017<\/strong>, <em>15<\/em>, 7072<span class=\"cit-pageRange\">\u2013<\/span>7087.<\/p>\n<p style=\"text-align: left;\">[56] <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523417302234\">In situ\u00a0targeted activation of a glucuronide prodrug using ultrasound-triggered release of composite droplets<\/a>.\u00a0Marine Bezagu, Jonathan\u00a0Clarhaut, Brigitte Renoux, Fabrice Monti, Mickael Tanter, Patrick Tabeling,* Janine Cossy,* Olivier Couture, S\u00e9bastien Papot<span style=\"line-height: 10px;\">,*\u00a0<\/span>Stellios Arseniyadis*<span style=\"line-height: 10px;\">\u00a0<em>Eur. J. Med. Chem<\/em>. <strong>2017<\/strong>,\u00a0<em>142, 2<span class=\"cit-pageRange\">\u2013<\/span>7.<\/em><\/span><\/p>\n<p style=\"text-align: left;\"><img decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/ars.els-cdn.com\/content\/image\/1-s2.0-S0223523417302234-fx1.jpg\" alt=\"Image 1\" height=\"200\" \/><\/p>\n<p style=\"text-align: left;\">[55] <em><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.6b02971?journalCode=orlef7\">A Pd-AAA approach to a-quaternary g-butyrolactones.<\/a>\u00a0<\/em>Marllon Nascimento de Oliveira, Jeremy Fournier, Stellios Arseniyadis,* Janine Cossy*\u00a0<em>Org. Lett.<\/em>\u00a0<strong>2017<\/strong>,\u00a0<span class=\"citation_volume\">19<\/span>, 14<span class=\"cit-pageRange\">\u2013<\/span>17.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-856 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2016\/12\/Marlon-1-1.png\" alt=\"\" width=\"574\" height=\"155\" \/><\/p>\n<p style=\"text-align: left;\">[54] <a href=\"http:\/\/www.lactualitechimique.org\/Catalyse-asymetrique-innovante-a-base-d-ADN\">Catalyse asym\u00e9trique innovante \u00e0 base d\u2019ADN<\/a>.\u00a0Stellios Arseniyadis,*\u00a0Nicolas Duchemin, Isabelle Heath-Apostolopoulos,\u00a0Michael Smietana*\u00a0<em>l'Actualit\u00e9 Chimique\u00a0<\/em><strong>2017<\/strong>, 417, 17<span class=\"cit-pageRange\">\u2013<\/span>27.<\/p>\n<p style=\"text-align: left;\">[53] <a href=\"http:\/\/www.lactualitechimique.org\/Des-produits-naturels-au-developpement-d-outils-synthetiques\">Des produits naturels au d\u00e9veloppement d\u2019outils synth\u00e9tiques<\/a>. Stellios Arseniyadis <em>l'Actualit\u00e9 Chimique <strong>2016<\/strong>, 413, 7<span class=\"cit-pageRange\">\u2013<\/span>18<\/em>. <img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-823\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Pr\u00e9sentation1.jpg\" width=\"500\" height=\"280\" \/><\/p>\n<p style=\"text-align: left;\">[52] <a href=\"http:\/\/journal.frontiersin.org\/article\/10.3389\/fchem.2016.00034\/abstract\">Total synthesis of putative 11-<em>epi<\/em>-lyngbouilloside aglycon<\/a>. Amandine Kolleth, Julian Gebauer, Abdelatif ElMarrouni, Raphael Lebeuf, C\u00e9line Pr\u00e9vost, Eric Brohan,\u00a0Stellios Arseniyadis,* Janine Cossy* <em>Front. Chem<\/em>. <strong>2016<\/strong>,\u00a0<em>4,<\/em>\u00a0Article 34.<\/p>\n<p style=\"text-align: left;\">[51] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/9781118754085.ch2\">Synthesis of\u00a0polyketides<\/a>. Cyril Bressy, Michael Smietana, Erica Benedetti, Stellios\u00a0Arseniyadis in\u00a0<em>From\u00a0Biosynthesis to Total Synthesis<\/em>, (Ed. A.\u00a0L. Zografos), Wiley <strong>2016<\/strong>, ch 2, 19<span class=\"cit-pageRange\">\u2013<\/span>129.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-863 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2016\/12\/Zographos.jpg\" alt=\"\" width=\"259\" height=\"337\" \/><\/p>\n<p style=\"text-align: left;\">[50] <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/cc\/c6cc03540j#!divAbstract\">Expanding biohybrid-mediated asymmetric catalysis into the realm of RNA<\/a>. Nicolas Duchemin, Erica Benedetti, Lucas Bethge, Stefan Vonhoff, Sven Klussmann, Jean-Jacques Vasseur, Janine Cossy, Michael Smietana,*\u00a0Stellios Arseniyadis*\u00a0<em>Chem. Commun<\/em>.\u00a0<strong>2016<\/strong>,\u00a0<em>52<\/em>, 8604<span class=\"cit-pageRange\">\u2013<\/span>8607.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-860 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2016\/12\/RNA.png\" width=\"700\" height=\"189\" \/><\/p>\n<p style=\"text-align: left;\"><span style=\"color: #000000;\">[49] <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acscatal.6b00495\">Design, synthesis and binding affinity evaluation of Hoechst 33258 derivatives for the development of sequence-specific DNA-based asymmetric catalysts<\/a>.\u00a0<\/span>Karen Amirbekyan, Nicolas Duchemin, Erica Benedetti, Rinah Joseph, Aude Colon, Shiraz A. Markarian, Lucas Bethge, Stefan Vonhoff, Sven Klussmann, Janine Cossy, Jean-Jacques Vasseur, Stellios Arseniyadis,* Michael Smietana* <em>ACS Catal<\/em>. <strong>2016<\/strong>,\u00a0<em><span class=\"citation_volume\">6<\/span><\/em>, 3096<span class=\"cit-pageRange\">\u2013<\/span>3105.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-855 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2016\/12\/Hoechst.png\" width=\"700\" height=\"197\" \/><\/p>\n<p style=\"text-align: left;\">[48] <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/cc\/c6cc08171a\">Selective Tsuji-Trost type C-allylation of hydrazones: A\u00a0straightforward entry into 4,5-dihydro pyrazoles<\/a>. Hachemia Elhachemia, Martin Cattoen, Marie Cordier, Janine Cossy, Stellios\u00a0Arseniyadis, Hocine Ilitki*, Laurent El Ka\u00efm*\u00a0<em>Chem. Commun<\/em>.\u00a0<strong>2016<\/strong>,\u00a0<em>52<\/em>, 14490<span class=\"cit-pageRange\">\u2013<\/span>14493.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-829\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Pyrazoles.png\" width=\"800\" height=\"194\" \/><\/p>\n<p style=\"text-align: left;\"><span style=\"color: #000000;\">[47] <\/span><a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2015\/lc\/c5lc00247h#!divAbstract\">A fast and switchable microfluidic mixer based on ultrasound-induced vaporization of perfluorocarbon<\/a>.\u00a0Marine Bezagu, Stellios Arseniyadis,* Janine\u00a0Cossy,* Olivier Couture, Mickael Tanter, Fabrice\u00a0Monti, Patrick\u00a0Tabeling* <em>Lab Chip\u00a0<\/em><strong>2015<\/strong><em>, 15,<\/em> 2025<span class=\"cit-pageRange\">\u2013<\/span>2029.<\/p>\n<p style=\"text-align: left;\"><span style=\"color: #000000;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-672\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Micromixer.png\" width=\"600\" height=\"180\" \/><\/span><\/p>\n<p style=\"text-align: left;\"><span style=\"color: #000000;\">[46] <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2014\/CC\/C4CC10190A#!divAbstract\">DNA-cellulose: An economical, fully recyclable and highly effective chiral biomaterial for asymmetric catalysis<\/a>. Erica Benedetti, Nicolas Duchemin, Lucas Bethge, Stefan Vonhoff, Sven Klussmann, Jean-Jacques Vasseur, Janine Cossy, Michael Smietana,* Stellios Arseniyadis* <em>Chem. Commun<\/em>. <strong>2015<\/strong>, <em>51<\/em>, 6076<span class=\"cit-pageRange\">\u2013<\/span>6079. Highlighted in <em><a href=\"https:\/\/www.chemistryworld.com\/research\/exploiting-the-chirality-of-dna\/8233.article\">Chemistry World<\/a><\/em>\u00a0and in the <a href=\"https:\/\/www.cnrs.fr\/inc\/communication\/direct_labos\/smietana2.htm\">CNRS website<\/a>.<\/span><\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-676\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Supported-DNA2.png\" alt=\"Supported DNA\" width=\"600\" height=\"231\" \/><\/p>\n<p style=\"text-align: left;\">[45] <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402014008862\">Recent developments in alkyne borylations<\/a>. Renaud Barberon,\u00a0Erica Benedetti, Jean-Jacques Vasseur, Janine Cossy,\u00a0Stellios\u00a0Arseniyadis,* Michael\u00a0Smietana,* <em>Tetrahedron<\/em> <strong>2014<\/strong>,\u00a0<i>70<\/i>, 8431<span class=\"cit-pageRange\">\u2013<\/span>8452.<\/p>\n<p style=\"text-align: left;\">[44] <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja5019354\">High spatiotemporal control of spontaneous reactions using ultrasound-triggered composite droplets<\/a>. Marine Bezagu, Claudia Errico, Victor Chaulot-Talmon, Fabrice Monti, Mickael Tanter, Patrick Tabeling,* Janine Cossy,* Stellios Arseniyadis,* Olivier\u00a0Couture, <em>J. Am. Chem. Soc<\/em>. <strong>2014<\/strong>, <em>136<\/em>, 7205<span class=\"cit-pageRange\">\u2013<\/span>7208. Highlighted in the <a href=\"https:\/\/www.cnrs.fr\/inc\/communication\/direct_labos\/arseniyadis.htm\">CNRS website<\/a>.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-852\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2016\/12\/Droplets-JACS.png\" width=\"700\" height=\"189\" \/><\/p>\n<p style=\"text-align: left;\">[43] <a href=\"https:\/\/www.thieme-connect.com\/ejournals\/abstract\/10.1055\/s-0033-1338987\">Palladium-catalyzed allylic alkylation of allyl dienol carbonates: Reactivity, regioselectivity, enantioselectivity and synthetic applications.<\/a>\u00a0Stellios Arseniyadis,*\u00a0J\u00e9r\u00e9my Fournier, Thangavelu Saravanan, Oscar Lozano, S\u00e9bastien Prevost, Alexis Archambeau, Candice Menozzi, Janine Cossy*\u00a0<i>Synlett<\/i> <strong>2013<\/strong>, 2350<span class=\"cit-pageRange\">\u2013<\/span>2364. Special issue for the\u00a0<em id=\"__mceDel\">5<sup>th\u00a0<\/sup>Edition of the Young Investigator Workshop <\/em>held in Marseille (invited article).<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Synlett-review.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-572\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Synlett-review.png\" alt=\"Synlett review\" width=\"600\" height=\"230\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[42] <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201306232\/abstract\">DNA vs. mirror image DNA: A universal approach to tune the absolute configuration in DNA-based asymmetric catalysis<\/a>. Jocelyn Wang, Erica Benedetti, Lucas Bethge, Stefan Vonhoff, Sven Klussmann, Jean-Jacques Vasseur, Janine Cossy, Michael\u00a0Smietana,* Stellios Arseniyadis* <i>Angew. Chem. Int. Ed.<\/i>\u00a0<strong>2013<\/strong>,\u00a0<i>52<\/i>, 11546<span class=\"cit-pageRange\">\u2013<\/span>11549. Highlighted in the <a href=\"https:\/\/www.cnrs.fr\/inc\/communication\/direct_labos\/smietana.htm\">CNRS website<\/a>.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/L-DNA13.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-535\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/L-DNA13.png\" alt=\"L-DNA\" width=\"600\" height=\"175\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[41] <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/cc\/c3cc45453c#!divAbstract\">Non-enzymatic acylative kinetic resolution of primary allylic amines<\/a>. Amandine Kolleth, Martin Cattoen, Stellios Arseniyadis,* Janine Cossy* <i>Chem. Commun.<\/i><b>\u00a0<\/b><strong>2013<\/strong><b>, <\/b><i>49<\/i>, 9338<span class=\"cit-pageRange\">\u2013<\/span>9340.<\/p>\n<p style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-542\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/KR-Chem-Comm-allylamine1.png\" width=\"600\" height=\"145\" \/><\/p>\n<p style=\"text-align: left;\">[40] <a href=\"http:\/\/naturalproduct.us\">Lyngbouilloside and related macrolides from marine cyanobacteria.<\/a> Abdelatif ElMarrouni, Amandine Kolleth, Raphael Lebeuf, Julian Gebauer, S\u00e9bastien Prevost, Montserrat Heras, Stellios Arseniyadis,* Janine Cossy* <em>Natural Product Communications <\/em><strong>2013<\/strong>, <em>8<\/em>, 965<span class=\"cit-pageRange\">\u2013<\/span>972.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Lyngbouilloside-copy.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-214\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Lyngbouilloside-copy.png\" width=\"600\" height=\"168\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[39] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/9783527658862.ch41\">Regio\u2010 and position selective reactions and desymmetrizations<\/a>.\u00a0<b><\/b>Alan C. Spivey,* Stellios Arseniyadis* in\u00a0<i>Comprehensive Enantioselective Organocatalysis<\/i>, Ed. P. Dalko, Wiley-VCH <strong>2013<\/strong>, Vol 3, Chapter 41, 1225<span class=\"cit-pageRange\">\u2013<\/span>1284.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Dalko.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-215\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Dalko.jpg\" alt=\"\" width=\"259\" height=\"367\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[38] <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ange.201206368\/abstract\">Palladium-catalyzed asymmetric allylic alkylation of cyclic dienol carbonates: Efficient route to enantioenriched g-butenolides bearing an all-carbon a-quaternary stereogenic center<\/a>. Jeremy Fournier, Oscar Lozano, Candice Menozzi, Stellios Arseniyadis,* Janine Cossy* <em>Angew. Chem. Int. Ed.<\/em> <strong>2013<\/strong> <em>52<\/em>, 1257<span class=\"cit-pageRange\">\u2013<\/span>1261 (Highlighted in <em>Synfacts <\/em>2013, <em>4<\/em>, 409<em>).<\/em><\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Pd-AAA-211.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-131\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Pd-AAA-211.png\" width=\"600\" height=\"137\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[37] <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlepdf\/2012\/cc\/c2cc35719d\">Kinetic resolution of propargylamines via a highly enantioselective non-enzymatic <em>N<\/em>-acylation process<\/a>. Amandine Kolleth, Sarah Christoph, Stellios Arseniyadis,* Janine Cossy*<em> Chem. Commun.<\/em> <strong>2012<\/strong>, <em>48<\/em>, 10511<span class=\"cit-pageRange\">\u2013<\/span>10513.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Propargylamine-KR-252.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-140\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Propargylamine-KR-252.png\" width=\"600\" height=\"159\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[36] <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlepdf\/2012\/cc\/c2cc35721f\">Catalysis-based enantioselective total synthesis of myxothiazole Z, (14<em>S<\/em>)-melithiazole G and (14<em>S<\/em>)\u2011cystothiazole F<\/a>. Aude Colon, Thomas J. Hoffman, Julian Gebauer, Jyotirmayee Dash, James H. Rigby, Stellios\u00a0Arseniyadis,* Janine\u00a0Cossy* <em>Chem. Commun.<\/em> <strong>2012<\/strong>,<em>48<\/em>, 10508<span class=\"cit-pageRange\">\u2013<\/span>10510.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Myxothiazole-Z-212.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-134\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Myxothiazole-Z-212.png\" width=\"600\" height=\"136\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[35] <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201202486\/abstract?systemMessage=Wiley+Online+Library+will+be+disrupted+on+11+May+from+10%3A00-12%3A00+BST+%2805%3A00-07%3A00+EDT%29+for+essential+maintenance\">A modular and scalable one-pot synthesis of polysubstituted furans<\/a>. Jeremy Fournier, Stellios Arseniyadis,* Janine Cossy* <em>Angew. Chem. Int. Ed.<\/em> <strong>2012<\/strong>, <em>51<\/em>, 7562<span class=\"cit-pageRange\">\u2013<\/span>7566.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Furans-243.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-138\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Furans-243.png\" width=\"600\" height=\"129\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[34] <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/9781118342886.ch16\">DNA as a tool for molecular discovery<\/a>. Michael Smietana,* Jean-Jacques Vasseur, Janine Cossy, Stellios Arseniyadis* in <em>Modern Tools for the Synthesis of Complex Bioactive Molecules, <\/em>(Eds.: J. Cossy, S. Arseniyadis), John Wiley &amp; Sons, Inc., Hoboken, NJ, USA. <strong>2012<\/strong>, 539<span class=\"cit-pageRange\">\u2013<\/span>556.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Modern-tools1.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-219\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Modern-tools1.jpg\" alt=\"\" width=\"259\" height=\"414\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[33] <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/ol203064r\">Total synthesis of nominal lyngbouilloside aglycon<\/a>. Abdelatif ElMarrouni, Raphael Lebeuf, Julian Gebauer, Montserrat Heras, Stellios Arseniyadis,* Janine\u00a0Cossy* <em>Org.\u00a0Lett.<\/em> <strong>2012<\/strong>, <em>14<\/em>, 314<span class=\"cit-pageRange\">\u2013<\/span>317.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Lyngbouilloside.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-141\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Lyngbouilloside.png\" width=\"600\" height=\"189\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[32] <a href=\"http:\/\/onlinelibrary.wiley.com\/book\/10.1002\/047084289X\/homepage\/WhatsNew.html\">2,6-bis[(4<em>S<\/em>)-4,5-Dihydro-4-(1-methylethyl)-5,5-diphenyl-2-oxazolyl] pyridine<\/a> in <em>electronic Encyclopedia of Organic Reagents <\/em>(e-EROS), Wiley-VCH, <strong>2011<\/strong>. Stellios Arseniyadis, Cyril Bressy.<\/p>\n<p style=\"text-align: left;\">[31] <a href=\"http:\/\/onlinelibrary.wiley.com\/book\/10.1002\/047084289X\/homepage\/WhatsNew.html\"><em>N<\/em>-[(1<em>S<\/em>)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-2-pyrrolidinecarbox amide<\/a> in <em>electronic Encyclopedia of Organic Reagents <\/em>(e-EROS), Wiley-VCH, <strong>2011<\/strong>. Stellios Arseniyadis, Cyril Bressy.<\/p>\n<p style=\"text-align: left;\">[30] <a href=\"http:\/\/cccc.uochb.cas.cz\/76\/10\/1239\/\">Studies towards the <em>N<\/em>-acylative kinetic resolution of NOBIN<\/a>. Stellios Arseniyadis, Mohan Mahesh, Paul McDaid, Thomas Hampel, Stephen G. Davey, Alan C. Spivey* <em>Coll. Czech. Chem. Commun.<\/em> <strong>2011<\/strong>, <em>76<\/em>, 1239<span class=\"cit-pageRange\">\u2013<\/span>1253.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/CCCC.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-293\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/CCCC.jpg\" alt=\"\" width=\"259\" height=\"363\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[29] <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403911000463\">A concise approach towards the synthesis of WS75624 A and WS75624 B via the cross-metathesis of vinyl-functionalized thiazoles.<\/a> Jyotirmayee Dash, Bruno Melillo, Stellios Arseniyadis,* Janine Cossy* <em>Tetrahedron Lett. <\/em><strong>2011<\/strong>, <em>52<\/em>, 2246<span class=\"cit-pageRange\">\u2013<\/span>2249 (Special issue in honour of Professor Harry H. Wasserman on the occasion of his 90<sup>th<\/sup> birthday).<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/WS75624-A-B.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-143\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/WS75624-A-B.png\" width=\"600\" height=\"119\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[28] <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jo1017487\">Expedient synthesis of a stereoisomer of acremolide B<\/a>. Abdelatif ElMarrouni, Aya Fukuda, Montserrat Heras, Stellios Arseniyadis,* Janine\u00a0Cossy* <em>J. Org. Chem. <\/em><strong>2010<\/strong>, <em>75<\/em>, 8478<span class=\"cit-pageRange\">\u2013<\/span>8486.<a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Acremolide-B2.png\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-346 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Acremolide-B2.png\" width=\"600\" height=\"220\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[27] <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/ol101659y\">Two concise total syntheses of (-)-bitungolide F<\/a>. Abdelatif ElMarrouni, Shyamsunder R. Joolakanti, Aude Colon, Montserrat Heras, Stellios Arseniyadis,* Janine\u00a0Cossy* <em>Org. Lett. <\/em><strong>2010<\/strong>, <em>12<\/em>, 4074<span class=\"cit-pageRange\">\u2013<\/span>4077.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Bitungolide-F5.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-297\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Bitungolide-F5.png\" width=\"600\" height=\"119\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[26] <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol101145t\">Stereoselective synthesis of the C1\u2011C11 and C12\u2011C34 fragments of mycalolide A<\/a>. Thomas J. Hoffman, Amandine Kolleth, James H. Rigby, Stellios\u00a0Arseniyadis,* Janine Cossy* <em>Org. Lett. <\/em><strong>2010<\/strong>, <em>12<\/em>, 3348<span class=\"cit-pageRange\">\u2013<\/span>3351.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/mycalolide.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-236\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/mycalolide.png\" width=\"600\" height=\"205\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[25] <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja100740t\">Total synthesis and structural revision of vannusals A and B. Synthesis of the originally assigned structure of Vannusal B<\/a>. K.\u00a0C.\u00a0Nicolaou,* Adrian Ortiz, Hongjun Zhang, Philippe Dagneau, Andreas Lanver, Michael P. Jennings, Stellios\u00a0Arseniyadis, Raffaella Faraoni, Dimitrios E. Lizos <em>J. Am. Chem. Soc. <\/em><strong>2010<\/strong>, <em>132<\/em>, 7138<span class=\"cit-pageRange\">\u2013<\/span>7152.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/vannusal.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-227\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/vannusal.gif\" alt=\"\" width=\"400\" height=\"161\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[24] <a href=\"http:\/\/link.springer.com\/content\/pdf\/10.1007%2F978-3-642-02815-1_25.pdf\">Amine, alcohol &amp; phosphine catalysts for acyl transfer reactions<\/a>. Alan Spivey,* Stellios Arseniyadis* <em>Topics in Current Chemistry: Asymmetric Organocatalysis<\/em>, Ed. B. List, Springer Verlag <strong>2010<\/strong>, Vol 291, Chapter 25, pp 233<span class=\"cit-pageRange\">\u2013<\/span>280.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Topics.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-289\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Topics.jpg\" alt=\"\" width=\"259\" height=\"393\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[23] <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol901846g\">Straightforward synthesis of the near-infrared fluorescent voltage-sensitive dye RH1691 and analogues thereof<\/a>. Rapha\u00ebl Lebeuf, Isabelle F\u00e9r\u00e9zou, Jean Rossier,Stellios\u00a0Arseniyadis,* Janine Cossy* <em>Org. Lett. <\/em><strong>2009<\/strong>, <em>11<\/em>, 4822<span class=\"cit-pageRange\">\u2013<\/span>4825.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/RH-1691.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-241\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/RH-1691.png\" width=\"600\" height=\"247\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[22] <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol900893e\">Enantioselective organocatalytic conjugate reduction of b-azole a,b-unsaturated aldehydes<\/a>. Thomas J. Hoffman, Jyotirmayee Dash, James H. Rigby, Stellios Arseniyadis,* Janine Cossy* <em>Org. Lett. <\/em><strong>2009<\/strong>, <em>11<\/em>, 2756<span class=\"cit-pageRange\">\u2013<\/span>2759.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Organocatalysis2.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-349\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Organocatalysis2.png\" width=\"600\" height=\"103\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[21] <a href=\"https:\/\/www.thieme-connect.de\/ejournals\/pdf\/10.1055\/s-0028-1087910.pdf?update=true\">One-pot hydrosilylation\/RCM\/protodesilylation: Application to the synthesis of w-alkenyl a,b-unsaturated lactones.<\/a> Cyril Bressy, Fr\u00e9d\u00e9ric Barggigia, Mathieu Guyonnet, Stellios Arseniyadis, Janine Cossy* <em>Synlett<\/em>, <strong>2009<\/strong>, 565<span class=\"cit-pageRange\">\u2013<\/span>568.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Hydrosilylation-17.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-286\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Hydrosilylation-17.png\" width=\"600\" height=\"132\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[20] <a href=\"https:\/\/www.thieme-connect.com\/ejournals\/pdf\/10.1055\/s-0028-1087641.pdf\">Asymmetric pentenylation of aldehydes: A new benchmark for the preparation of ethyl-substituted homoallylic alcohols<\/a>. Ravindra P. Sonawane, Shyamsunder R. Joolakanti, Stellios Arseniyadis,* Janine Cossy* <em>Synlett<\/em> <strong>2009<\/strong>, 213<span class=\"cit-pageRange\">\u2013<\/span>216.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Pentenylation-141.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-351\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Pentenylation-141.png\" width=\"600\" height=\"123\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[19] <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.200802423\/pdf\">Asymmetric total synthesis of the immunosuppressant (-)-pironetin<\/a>. Cyril Bressy, Jean-Pierre Vors, Stefan Hillebrand, Stellios Arseniyadis, Janine Cossy* <em>Angew. Chem, Int. Ed. <\/em><strong>2008<\/strong>, <em>47<\/em>, 10137<span class=\"cit-pageRange\">\u2013<\/span>10140.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Pironetine.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-284\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Pironetine.png\" width=\"600\" height=\"172\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[18] <a href=\"https:\/\/www.thieme-connect.de\/DOI\/DOI?10.1055\/s-0028-1083511\">Formal synthesis of leustroducsin B<\/a>. Jo\u00eblle Mo\u00efse, Ravindra P. Sonawane, Camilla Corsi, Sebastian V. Wendeborn, Stellios Arseniyadis,* Janine Cossy* <em>Synlett<\/em> <strong>2008<\/strong>, 2617<span class=\"cit-pageRange\">\u2013<\/span>2620. <a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Leustroducsin-B1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-367\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Leustroducsin-B1.png\" width=\"650\" height=\"195\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[17] <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ejoc.200800203\/pdf\">Total synthesis of cystothiazole A by microwave-assisted olefin cross-metathesis<\/a>. Julian Gebauer, Stellios Arseniyadis,* Janine Cossy* <em>Eur. J. Org. Chem.<\/em> <strong>2008<\/strong>, 2701<span class=\"cit-pageRange\">\u2013<\/span>2704.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Cystothiazole-A.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-362\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Cystothiazole-A.png\" width=\"700\" height=\"188\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[16] <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jo702305g\">Synthesis of vinyl-functionalized oxazoles by olefin cross-metathesis<\/a>. Thomas J. Hoffman, James H. Rigby, Stellios Arseniyadis, Janine Cossy* <em>J. Org. Chem. <\/em><strong>2008<\/strong>, <em>73<\/em>, 2400<span class=\"cit-pageRange\">\u2013<\/span>2403.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Oxazole-CM-91.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-342\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Oxazole-CM-91.png\" width=\"650\" height=\"123\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[15] <a href=\"https:\/\/www.thieme-connect.de\/DOI\/DOI?10.1055\/s-2008-1042805\">Facile synthesis of the C1\u2013C13 fragment of lyngbouilloside<\/a>. Julian Gebauer, Stellios Arseniyadis,* Janine Cossy* S<em>ynlett<\/em> <strong>2008<\/strong>, 712<span class=\"cit-pageRange\">\u2013<\/span>714.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Lyngbouilloside-11.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-370\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Lyngbouilloside-11.png\" width=\"700\" height=\"161\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[14] <a href=\"https:\/\/www.thieme-connect.com\/ejournals\/abstract\/10.1055\/s-2007-1000879\">Non-enzymatic kinetic resolution of amines in ionic liquids<\/a>. Cyrille Sabot, Pithani V. Subhash, Alain Valleix, Stellios Arseniyadis,* Charles Mioskowski,* <em>Synlett<\/em> <strong>2008<\/strong>, 268<span class=\"cit-pageRange\">\u2013<\/span>272.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/KR-Chem-Synlett.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-404\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/KR-Chem-Synlett.png\" width=\"600\" height=\"127\" \/><\/a><\/p>\n<p>[13] <a href=\"https:\/\/patents.google.com\/patent\/WO2007062288A2\/en?oq=WO2007062288\">Chemical synthesis of a highly potent epothilone<\/a>. Kyriakos C. Nicolaou, Benjamin Pratt, Stellios Arseniyadis (International publication number: WO2007062288A2, International publication date: 31\/05\/2007).<\/p>\n<p style=\"text-align: left;\">[12]\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol701459j\">A concise total synthesis of melithiazole C<\/a>. Julian Gebauer, Stellios Arseniyadis, Janine Cossy* <em>Org. Lett. <\/em><strong>2007<\/strong>, <em>9<\/em>, 3425<span class=\"cit-pageRange\">\u2013<\/span>3427.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Melithiazole-C.png\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-360 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Melithiazole-C.png\" width=\"650\" height=\"174\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[11] <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/cmdc.200600206\/pdf\">The chemistry and biology of epothilones \u2013 The wheel keeps turning<\/a>. Karl-Heinz Altmann,* Bernhard Pfeiffer, Stellios Arseniyadis, Benjamin A. Pratt, K. C. Nicolaou* <em>ChemMedChem<\/em> <strong>2007<\/strong>, 396<span class=\"cit-pageRange\">\u2013<\/span>423.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Epothilone-review.gif\"><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-356 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Epothilone-review.gif\" alt=\"\" width=\"329\" height=\"227\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[10]\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol0703940\">Cross-Metathesis between a-methylene-g-butyrolactone and olefins: A dramatic additive effect<\/a>. Jo\u00eblle\u00a0Mo\u00efse, Stellios Arseniyadis,* Janine Cossy* <em>Org. Lett. <\/em><strong>2007<\/strong>, 9, 1695<span class=\"cit-pageRange\">\u2013<\/span>1698.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Lactone-CM.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-347\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Lactone-CM.png\" width=\"650\" height=\"128\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[9]\u00a0<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.200600509\/pdf\">Synthesis\u00a0of\u00a0vinyl-functionalized thiazoles by cross-metathesis and tandem Stille coupling\/cross-metathesis<\/a>. Jyotirmayee Dash, Stellios Arseniyadis, Janine Cossy* <em>Adv. Synth. Cat.<\/em> <strong>2007<\/strong>, <em>349<\/em>, 152<span class=\"cit-pageRange\">\u2013<\/span>156.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Thiazole-CM1.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-344\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Thiazole-CM1.png\" width=\"650\" height=\"123\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[8]\u00a0<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/cmdc.200500056\/pdf\">Molecular design and chemical synthesis of a highly potent epothilone<\/a>. K. C. Nicolaou,* Benjamin A. Pratt, Stellios Arseniyadis, Markus Wartmann, Aurora O\u2019Brate, Paraskevi Giannakakou <em>ChemMedChem<\/em> <strong>2006<\/strong>, <em>1<\/em>, 41<span class=\"cit-pageRange\">\u2013<\/span>44.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Epothilone.gif\"><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-354 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Epothilone.gif\" alt=\"\" width=\"259\" height=\"335\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[7]\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402005015565\">Rapid,\u00a0room-temperature acylative kinetic resolution of\u00a0<em>sec<\/em>-alcohols using atropisomeric 4-aminopyridine\/triphenylphosphine catalysis<\/a>. Alan C. Spivey,* Stellios Arseniyadis, Tomasz Fekner, Adrian Maddaford, David P. Leese <em>Tetrahedron<\/em> <strong>2006<\/strong>, <em>62<\/em>, 295<span class=\"cit-pageRange\">\u2013<\/span>301.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Tetrahedron-Spivey.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-393\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Tetrahedron-Spivey.png\" width=\"650\" height=\"150\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[6]\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2005\/CC\/b504200c\">Unprecedented, fully recyclable, solid-supported reagent for the kinetic resolution of racemic amines through enantioselective <em>N-<\/em>acetylation<\/a>. Stellios Arseniyadis, Pithani V. Subhash, Alain Valleix, Alain Wagner,* Charles Mioskowski* <em>Chem. Commun.<\/em> <strong>2005<\/strong>, <em>26<\/em>, 3310<span class=\"cit-pageRange\">\u2013<\/span>3312 (Highlighted in <em>Synfacts <\/em>2005, <em>1<\/em>, 170<em>).<\/em><\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Supported-KR.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-375\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Supported-KR.png\" width=\"650\" height=\"207\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[5]\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja051302%2B\">Tuning the enantioselective <em>N<\/em>-acetylation of racemic amines: A spectacular salt effect<\/a>. Stellios Arseniyadis, Pithani V. Subhash, Alain Valleix, Suju P. Mathew,Donna G. Blackmond, Alain Wagner,* Charles Mioskowski* <em>J. Am. Chem. Soc.<\/em> <strong>2005<\/strong>, <em>127<\/em>, 6138<span class=\"cit-pageRange\">\u2013<\/span>6139.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/KR-JACS.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-382\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/KR-JACS.png\" width=\"650\" height=\"173\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[4]\u00a0<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.200460373\/pdf\">Nucleophilic catalysis by 4-(dialkylamino)pyridines revisited\u00a0-\u00a0The search for optimal reactivity and selectivity<\/a>. Alan C. Spivey,* Stellios Arseniyadis <em>Angew. Chem. Int. Ed.<\/em> <strong>2004<\/strong>, <em>43<\/em>, 5436<span class=\"cit-pageRange\">\u2013<\/span>5441.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Highlight.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-399\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Highlight.gif\" alt=\"\" width=\"259\" height=\"335\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[3]\u00a0<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.200453956\/abstract\">Kinetic resolution of amines: A chemoselective and highly enantioselective acetylating agent with a unique solvent-induced reversal of stereoselectivity<\/a>. Stellios Arseniyadis, Alain Valleix, Alain Wagner,* Charles Mioskowski* <em>Angew. Chem. Int. Ed.<\/em> <strong>2004<\/strong>, <em>43<\/em>, 3314<span class=\"cit-pageRange\">\u2013<\/span>3317.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/KR-Chem-Angew.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-401\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/KR-Chem-Angew.png\" width=\"650\" height=\"176\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[2]\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403904000929\">Resin bound 4-phenyl-1,2-dihydroquinoline (DHQ): An new safety-catch linker for solid phase organic synthesis (SPOS).<\/a> Stellios Arseniyadis, Alain Wagner,* Charles Mioskowski* <em>Tetrahedron Lett. <\/em><strong>2004<\/strong>, <em>45<\/em>, 2251<span class=\"cit-pageRange\">\u2013<\/span>2253.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Safety-catch-linker.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-397\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Safety-catch-linker.png\" width=\"650\" height=\"143\" \/><\/a><\/p>\n<p style=\"text-align: left;\">[1]\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403902021925\">A\u00a0straightforward preparation of amino-polystyrene resin from Merrifield resin<\/a>. Stellios Arseniyadis, Alain Wagner,* Charles Mioskowski* <em>Tetrahedron Lett<\/em>. <strong>2002<\/strong>, <em>43<\/em>, 9717<span class=\"cit-pageRange\">\u2013<\/span>9719.<\/p>\n<p style=\"text-align: left;\"><a href=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Aniline-resin.png\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-395\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2013\/04\/Aniline-resin.png\" width=\"650\" height=\"107\" \/><\/a><\/p>\n<p style=\"text-align: left;\"><strong>Patents<\/strong><\/p>\n<p><span lang=\"EN-US\">[2]<\/span><span lang=\"EN-US\"> <a href=\"https:\/\/patents.google.com\/patent\/WO2023156972A1\/en?oq=WO2023156972A1\">Palladium precatalyst embodiments for enantioselective chemical reactions and methods of making and using the same<\/a>. D. Leitch, Stellios Arseniyadis, Jingjun Huang (International publication number: WO2023156972A1, International publication date: 24\/08\/2023).<\/span><span lang=\"EN-US\"><br \/>\n<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2723 aligncenter\" src=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-2-300x58.jpg\" alt=\"\" width=\"601\" height=\"116\" srcset=\"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-2-300x58.jpg 300w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-2-1024x198.jpg 1024w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-2-768x148.jpg 768w, https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/wp-content\/uploads\/2024\/02\/Untitled-2.jpg 1358w\" sizes=\"auto, (max-width: 601px) 100vw, 601px\" \/><\/p>\n<p style=\"text-align: left;\">[1] Chemical synthesis of a highly potent epothilone. K. C. Nicolaou, K. C.; B. Pratt, S. Arseniyadis (International publication number: WO2007062288, International publication date: 31\/05\/2007).<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"<p>Submitted or in preparation: [104] Straightforward Access to Diversely Substituted Pyrrolidones via Pd-Catalysed Allylic Substitution of Nitroallyl Derivatives. Mansour Dol\u00e9 Kerim, Stellios Arseniyadis,* Laurent El Kaim* (in preparation). [103] Stereodivergent iridium-catalyzed asymmetric allylic alkylation of hydantoins. Yao-Rui Ma, Yibing Chen, Paul Clark, Avantika Hasija, Thibaud Bregent, Alexandre Jean, Pei\u2011Qiang Huang,* Guillaume Lef\u00e8vre,* Stellios Arseniyadis* (in [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-680","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/pages\/680","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=680"}],"version-history":[{"count":399,"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/pages\/680\/revisions"}],"predecessor-version":[{"id":2872,"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/pages\/680\/revisions\/2872"}],"wp:attachment":[{"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=680"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}