{"id":732,"date":"2024-04-08T07:12:35","date_gmt":"2024-04-08T07:12:35","guid":{"rendered":"https:\/\/mint-team.fr\/?page_id=732"},"modified":"2024-04-08T07:19:11","modified_gmt":"2024-04-08T07:19:11","slug":"publications_before2015","status":"publish","type":"page","link":"https:\/\/mint-team.fr\/index.php\/publications_before2015\/","title":{"rendered":"Publications  before 2015"},"content":{"rendered":"\n<ul>\n<li class=\"has-medium-font-size\" style=\"font-style:normal;font-weight:500;letter-spacing:2px;text-decoration:underline;text-transform:none\">2014<\/li>\n<\/ul>\n\n\n\n<figure class=\"wp-block-table has-medium-font-size\"><table style=\"border-style:none;border-width:0px\"><tbody><tr><td>Melnyk, O.; Ollivier, N.; Besret, S.; Melnyk, P. Phenylthiocarbamate or N -carbothiophenyl group chemistry in peptide synthesis and bioconjugation. <em>Bioconjugate Chem.<\/em> <strong>2014<\/strong>, <em>25<\/em>, 629-639<\/td><\/tr><tr><td>Melnyk, O.; Agouridas, V. From protein total synthesis to peptide transamidation and metathesis: playing with the reversibility of N,S-acyl or N,Se-acyl migration reactions. <em>Curr. Opin. Chem. Biol. <\/em><strong>2014<\/strong>, <em>22<\/em>, 137-145<\/td><\/tr><tr><td>Ollivier, N.; Blanpain, A.; Boll, E.; Raibaut, L.; Drobecq, H.; Melnyk, O. Selenopeptide transamidation and metathesis. <em>Org. Lett. <\/em><strong>2014<\/strong>, <em>16<\/em>, 4032-4035<\/td><\/tr><tr><td>Besret, S.; Vicogne, J.; Dahmani, F.; Fafeur, V.; Desmet, R.; Drobecq, H.; Romieu, A.; Melnyk, P.; Melnyk, O. Thiocarbamate-linked polysulfonate-peptide conjugates as selective hepatocyte growth factor receptor binders. <em>Bioconjugate Chem.<\/em> <strong>2014<\/strong>, <em>25<\/em>, 1000-1010<\/td><\/tr><tr><td>Boll, E.; Drobecq, H.; Ollivier, N.; Raibaut, L.; Desmet, R.; Vicogne, J.; Melnyk, O. A novel PEG-based solid support enables the synthesis of &gt;50 amino-acid peptide thioesters and the total synthesis of a functional SUMO-1 peptide conjugate. <em>Chem. Sci. <\/em><strong>2014<\/strong>, <em>5<\/em>, 2017-2022<\/td><\/tr><tr><td>Ollivier, N.; Raibaut, L.; Blanpain, A.; Desmet, R.; Dheur, J.; Mhidia, R.; Boll, E.; Drobecq, H.; Pira, S.L.; Melnyk, O. Tidbits for the synthesis of bis(2-sulfanylethyl)amido (SEA) polystyrene resin, SEA peptides and peptide thioesters. <em>J. Pept. Sci. <\/em><strong>2014<\/strong>, <em>20<\/em>, 92-97<\/td><\/tr><tr><td>Pike, S. J.; Diemer, V.; Raftery, J.; Webb, S. J.; Clayden, J. Designing Foldamer-Foldamer Interactions in Solution: The Roles of Helix Length and Terminus Functionality in Promoting the Self-Association of Aminoisobutyric Acid Oligomers. <em>Chemistry<\/em> <strong>2014<\/strong>, <em>20<\/em>, 15981-15990.<\/td><\/tr><tr><td>Chaumeil, H.; Neuburger, M.; Jacques, P.; Tschamber, T.; Diemer, V.; Carr\u00e9, C. Conformational analysis of some pyridinium phenolates and synthetic precursors based on X-ray and IR characterisations. <em>Tetrahedron<\/em> <strong>2014<\/strong>,<em> 70<\/em>, 3116-3122.<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<ul>\n<li class=\"has-medium-font-size\" style=\"font-style:normal;font-weight:500;letter-spacing:2px;text-decoration:underline;text-transform:none\">2013<\/li>\n<\/ul>\n\n\n\n<figure class=\"wp-block-table has-medium-font-size\"><table style=\"border-style:none;border-width:0px\"><tbody><tr><td>El-Mahdi, O.; Melnyk, O. \u03b1-oxo aldehyde or glyoxylyl group chemistry in peptide bioconjugation. <em>Bioconjugate Chem.<\/em> <strong>2013<\/strong>,<em> 24<\/em>, 735-765<\/td><\/tr><tr><td>Raibaut, L.; Seeberger, P.; Melnyk, O. Bis(2-sulfanylethyl)amido peptides enable native chemical ligation at proline and minimize deletion side-product formation. <em>Org. Lett. <\/em><strong>2013<\/strong>, <em>15<\/em>, 5516-5519<\/td><\/tr><tr><td>Pira, S. L.; Boll, E.; Melnyk, O. Synthesis of peptide thioacids at neutral pH using bis(2-sulfanylethyl) amido peptide precursors. <em>Org. Lett. <\/em><strong>2013<\/strong>, <em>15<\/em>, 5346-5349<\/td><\/tr><tr><td>Raibaut, L.; Adihou, H.; Adihou, R.; Delmas, A. F.; Aucagne, V.; Melnyk, O. Highly efficient solid phase synthesis of large polypeptides by iterative ligations of bis(2-sulfanylethyl)amido (SEA) peptide segments. <em>Chem. Sci.<\/em> <strong>2013<\/strong>, <em>4<\/em>, 4061-4066<\/td><\/tr><tr><td>F\u00e9court, F.; Delpech, B.; Melnyk, O.; Crich, D. Se -(9-fluorenylmethyl) selenoesters : Preparation, reactivity, and use as convenient synthons for selenoacids. <em>Org. Lett. <\/em><strong>2013<\/strong>, <em>15<\/em>, 3758-3761<\/td><\/tr><tr><td>Raibaut, L.; Vicogne, J.; Leclercq, B.; Drobecq, H.; Desmet, R.; Melnyk, O. Total synthesis of biotinylated N domain of human hepatocyte growth factor. <em>Bioorg. Med. Chem. <\/em><strong>2013<\/strong>, <em>21<\/em>, 3486-3494<\/td><\/tr><tr><td>Mhidia, R.; Boll, E.; F\u00e9court, F.; Ermolenko, M.; Ollivier, N.; Sasaki, K.; Crich, D.; Delpech, B.; Melnyk, O. Exploration of an imide capture\/N,N-acyl shift sequence for asparagine native peptide bond formation. <em>Bioorg. Med. Chem.<\/em> <strong>2013<\/strong>, <em>21<\/em>, 3479-3485<\/td><\/tr><tr><td>Greene, A. E.; Agouridas, V.; Deniau, E. Cesium carbonate mediated aryl trflate esters&#8217; deprotection. <em>Tetrahedron Lett.<\/em> <strong>2013<\/strong>, <em>54<\/em>, 7078-7079<\/td><\/tr><tr><td>Vanderstraete, M.; Gouignard, N.; Ahier, A.; Morel, M.; Vicogne, J.; Dissous, C. The venus kinase receptor (VKR) family: Structure and evolution. <em>BMC Genomics<\/em> <strong>2013<\/strong>, <em>14<\/em>, 361<\/td><\/tr><tr><td>Brown, R. A.; Diemer, V.; Webb, S. J.; Clayden, J. End-to-end conformational communication through a synthetic purinergic receptor by ligand-induced helicity switching. <em>Nat. Chem.<\/em> <strong>2013<\/strong>,<em> 5<\/em>, 853-860.<\/td><\/tr><\/tbody><\/table><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Melnyk, O.; Ollivier, N.; Besret, S.; Melnyk, P. Phenylthiocarbamate or N -carbothiophenyl group chemistry in peptide synthesis and bioconjugation. Bioconjugate Chem. 2014, 25, 629-639 Melnyk, O.; Agouridas, V. From protein total synthesis to peptide transamidation and metathesis: playing with the reversibility of N,S-acyl or N,Se-acyl migration reactions. Curr. Opin. Chem. Biol. 2014, 22, 137-145 Ollivier,&hellip;&nbsp;<a href=\"https:\/\/mint-team.fr\/index.php\/publications_before2015\/\" class=\"\" rel=\"bookmark\">Read More &raquo;<span class=\"screen-reader-text\">Publications  before 2015<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"neve_meta_sidebar":"","neve_meta_container":"","neve_meta_enable_content_width":"","neve_meta_content_width":0,"neve_meta_title_alignment":"","neve_meta_author_avatar":"","neve_post_elements_order":"","neve_meta_disable_header":"","neve_meta_disable_footer":"","neve_meta_disable_title":"","_themeisle_gutenberg_block_has_review":false,"_ti_tpc_template_sync":false,"_ti_tpc_template_id":"","footnotes":""},"_links":{"self":[{"href":"https:\/\/mint-team.fr\/index.php\/wp-json\/wp\/v2\/pages\/732"}],"collection":[{"href":"https:\/\/mint-team.fr\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/mint-team.fr\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/mint-team.fr\/index.php\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/mint-team.fr\/index.php\/wp-json\/wp\/v2\/comments?post=732"}],"version-history":[{"count":1,"href":"https:\/\/mint-team.fr\/index.php\/wp-json\/wp\/v2\/pages\/732\/revisions"}],"predecessor-version":[{"id":740,"href":"https:\/\/mint-team.fr\/index.php\/wp-json\/wp\/v2\/pages\/732\/revisions\/740"}],"wp:attachment":[{"href":"https:\/\/mint-team.fr\/index.php\/wp-json\/wp\/v2\/media?parent=732"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}