Photocatalyst-free, metal-free, visible light-induced thiolation/pyridylation of styrenes using an electron donor–acceptor complex as a bifunctional reagent†
{"title":"Photocatalyst-free, metal-free, visible light-induced thiolation/pyridylation of styrenes using an electron donor–acceptor complex as a bifunctional reagent†","authors":"Jiaxuan Shen , Jincan Li , Meijun Chen , Yimin Chen","doi":"10.1039/d2qo01889f","DOIUrl":null,"url":null,"abstract":"<div><p>Herein, we report a visible light-induced photocatalytic protocol for the thiolation and pyridylation of styenes using a thiolate-based EDA complex as a bifunctional reagent. The reaction occurrs under mild conditions free of a photocatalyst, metal or external redox agent, possessing a broad substrate scope. The protocol can be practiced on the gram-scale, and late-stage functionalization of natural product- and drug-derived complex molecules is also possible.</p></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"10 5","pages":"Pages 1166-1172"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052411023005254","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract
Herein, we report a visible light-induced photocatalytic protocol for the thiolation and pyridylation of styenes using a thiolate-based EDA complex as a bifunctional reagent. The reaction occurrs under mild conditions free of a photocatalyst, metal or external redox agent, possessing a broad substrate scope. The protocol can be practiced on the gram-scale, and late-stage functionalization of natural product- and drug-derived complex molecules is also possible.