{"id":870,"date":"2017-01-10T03:04:17","date_gmt":"2017-01-10T03:04:17","guid":{"rendered":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/?p=870"},"modified":"2019-01-13T02:40:44","modified_gmt":"2019-01-13T02:40:44","slug":"latest-publications","status":"publish","type":"post","link":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/?p=870","title":{"rendered":"Latest Publications"},"content":{"rendered":"<ul>\n<li><em>Chem. Sci.<\/em>\u00a0<strong>2019<\/strong>, (<em>in press<\/em>). A rational quest for selectivity through precise ligand-positioning in the tandem DNA-catalysed Friedel-Crafts alkylation\/asymmetric protonation. Justine Mansot,\u00a0Sidonie Aubert,\u00a0Nicolas Duchemin,\u00a0Jean-Jacques Vasseur,\u00a0Stellios\u00a0Arseniyadis,\u00a0and Michael Smietana\u00a0<!--more--><\/li>\n<li><em>Org. Lett.<\/em>\u00a0<strong>2019<\/strong>, (<em>in press<\/em>). Asymmetric synthesis of \u03b1-quaternary \u03b3-lactams through palladium-catalyzed asymmetric allylic alkylation. Tao Song, Stellios Arseniyadis,* and Janine Cossy*\u00a0<!--more--><\/li>\n<li><em>Angew. Chem. Int. Ed.<\/em>\u00a0<strong>2018<\/strong>, (<em>in press<\/em>). <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,* and Stellios Arseniyadis*<!--more--><\/li>\n<li><em>Chem. Eur. J.<\/em>\u00a0<strong>2018<\/strong>, (<em>in press<\/em>). <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/chem.201800920\">Highly Enantioselective, Base-Free Synthesis of a-Quaternary\u00a0Succinimides through Catalytic Asymmetric Allylic Alkylation<\/a>.<em>\u00a0<\/em>Tao Song, Stellios Arseniyadis,* Janine Cossy*<!--more--><\/li>\n<li><em>Dalton Trans.<\/em>\u00a0<strong>2018<\/strong> (<em>in press<\/em>).\u00a0<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*<!--more--><\/li>\n<li><em>Chem. Eur. J\u00a0<\/em><strong>2018<\/strong>\u00a0(<em>in press<\/em>). \u00a0<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 b<sup>2,2<\/sup>\u2011Amino Acids<\/a>.<em>\u00a0<\/em>Marllon Nascimento de Oliveira, Stellios Arseniyadis,* Janine Cossy*<!--more--><\/li>\n<li><em>Adv. Synth. &amp; Catal<\/em>.<em>\u00a0<\/em><strong>2018<\/strong>\u00a0(<em>in press<\/em>).\u00a0<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/adsc.201701150?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-Hydroxyphosphonates: An\u00a0Expedient entry into Phosphono-oxaheterocycles<\/a>. M.\u00a0Dol\u00e9 Kerim,\u00a0M. Cattoen,\u00a0N. Fincias,\u00a0A. Dos Santos,\u00a0S. Arseniyadis,* L.\u00a0El Ka\u00efm*<!--more--><\/li>\n<li><em>Org. Biomol. Chem<\/em>.<em>\u00a0<\/em><strong>2017<\/strong>\u00a0(<em>in press<\/em>). <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/ob\/c7ob00176b#!divAbstract\">A decade of DNA-hybrid catalysis: from innovation to comprehension<\/a>. N. Duchemin, I. Heath-Apostolopoulos,\u00a0M. Smietana,*\u00a0S. Arseniyadis*<!--more--><\/li>\n<li><em>l\u2019Actualit\u00e9 Chimique\u00a0<strong>2017<\/strong>\u00a0(in press)\u00a0<\/em>Catalyse asym\u00e9trique innovante \u00e0 base d\u2019ADN.\u00a0S. Arseniyadis,*\u00a0N. Duchemin, I. Heath-Apostolopoulos,\u00a0M. Smietana*<!--more--><\/li>\n<li><em>Org. Lett.\u00a0<strong>2017<\/strong>,\u00a0<span class=\"citation_volume\">19<\/span>, 14-17.\u00a0<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>\u00a0M. Nascimento de Oliveira, J. Fournier, S. Arseniyadis,* J. Cossy*<!--more--><\/em><\/li>\n<li><em>ACS Catal<\/em>.\u00a0<strong>2016<\/strong>,\u00a0<em>6<\/em>, 3096-3105.\u00a0<span style=\"color: #000000;\"><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>K. Amirbekyan, N. Duchemin, E. Benedetti, R. Joseph, A. Colon, S. A. Markarian, L. Bethge, S. Vonhoff, S. Klussmann, J. Cossy, J.-J. Vasseur, S. Arseniyadis,* \u00a0M. Smietana*<\/li>\n<\/ul>\n<p><!--more--><\/p>\n<ul>\n<li><em>Chem. Commun<\/em>.\u00a0<strong>2016<\/strong>,\u00a0<em>52<\/em>, 14490-14493.\u00a0<a href=\"http:\/\/pubs.rsc.org\/-\/content\/articlelanding\/2016\/cc\/c6cc08171a#!divAbstract\">Selective Tsuji-Trost type C-allylation of hydrazones: A\u00a0straightforward entry into 4,5-dihydro pyrazoles<\/a>. H.\u00a0Elhachemia, M.\u00a0Cattoen, M.\u00a0Cordier, J.\u00a0Cossy, S.\u00a0Arseniyadis, H.\u00a0Ilitki*, L.\u00a0El Ka\u00efm*<\/li>\n<\/ul>\n<p><!--more--><\/p>\n<ul>\n<li><em>l&#8217;Actualit\u00e9 Chimique\u00a0<\/em><strong>2016<\/strong>,\u00a0413, 7-18.\u00a0<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>. S. Arseniyadis<\/li>\n<\/ul>\n<p><!--more--><\/p>\n<ul>\n<li><em>Chem. Commun.\u00a0<strong>2016<\/strong>,\u00a052, 8604-8607.\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/cc\/c6cc03540j#!divAbstract\">Expanding Biohybrid-mediated Asymmetric Catalysis into the Realm of RNA<\/a>. N.\u00a0Duchemin, E.\u00a0Benedetti, L.\u00a0Bethge, S.\u00a0Vonhoff, S.\u00a0Klussmann, J.-J.\u00a0Vasseur, J.\u00a0Cossy, M.\u00a0Smietana,*\u00a0S.\u00a0Arseniyadis*<\/em><\/li>\n<\/ul>\n<p><!--more--><\/p>\n<ul>\n<li><em>Front. Chem<\/em>.\u00a0<strong>2016<\/strong>,\u00a0<em>4,<\/em>\u00a0Article 34.\u00a0<a href=\"http:\/\/journal.frontiersin.org\/article\/10.3389\/fchem.2016.00034\/abstract\">Total synthesis of putative 11-<em>epi<\/em>-lyngbouilloside aglycon<\/a>. A.\u00a0Kolleth, J. Gebauer, A. ElMarrouni, R. Lebeuf, C. Pr\u00e9vost, E. Brohan,\u00a0S. Arseniyadis,* J. Cossy*<\/li>\n<\/ul>\n<p><!--more--><\/p>\n<ul>\n<li><a href=\"https:\/\/books.google.co.uk\/books?id=POTFCwAAQBAJ&amp;pg=PR7&amp;lpg=PR7&amp;dq=arseniyadis+bressy+smietana+benedetti&amp;source=bl&amp;ots=20mSXJB3bO&amp;sig=Hh38QpS7EL0R4IYwmH696XzYGsI&amp;hl=en&amp;sa=X&amp;ved=0ahUKEwjKvcXWxZHMAhVEuRQKHVbZCTAQ6AEIKTAC#v=onepage&amp;q=arseniyadis%20bressy%20smietana%20benedetti&amp;f=false\">Synthesis of\u00a0Polyketides<\/a>. C. Bressy, M. Smietana, E. Benedetti, S. Arseniyadis in\u00a0<em>From\u00a0Biosynthesis to Total Synthesis<\/em>, <em>Strategies and Tactics for Natural Products<\/em> (Ed. A.\u00a0L. Zografos), Wiley\u00a0<strong>2016,\u00a0<\/strong>Chap 2, pp 21-129<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Chem. Sci.\u00a02019, (in press). A rational quest for selectivity through precise ligand-positioning in the tandem DNA-catalysed Friedel-Crafts alkylation\/asymmetric protonation. Justine Mansot,\u00a0Sidonie Aubert,\u00a0Nicolas Duchemin,\u00a0Jean-Jacques Vasseur,\u00a0Stellios\u00a0Arseniyadis,\u00a0and Michael Smietana\u00a0<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-870","post","type-post","status-publish","format-standard","hentry","category-uncategorised"],"_links":{"self":[{"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/posts\/870","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/types\/post"}],"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=870"}],"version-history":[{"count":22,"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/posts\/870\/revisions"}],"predecessor-version":[{"id":1830,"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=\/wp\/v2\/posts\/870\/revisions\/1830"}],"wp:attachment":[{"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=870"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=870"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/arseniyadislab.sbcs.qmul.ac.uk\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=870"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}