{"title":"光氧化还原自由基休战-微笑重排n -亚砜酰丙烯酰胺与亚砜酰铵","authors":"Lin Tian , Pu Chen , Lindong Xiao , Huawen Huang","doi":"10.1039/d5cc03513a","DOIUrl":null,"url":null,"abstract":"<div><div>The visible light-induced Truce–Smiles rearrangement reaction of <em>N</em>-sulfinyl acrylamides with sulfoxonium ylides is herein reported. The reaction is performed under mild conditions by radical addition/aryl migration, allowing the synthesis of a range of valuable α-arylamides in moderate to good yields. The resultant α-aryl-γ-benzoylamides were converted by late-stage modification to a number of synthetically valuable derivatives.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 70","pages":"Pages 13141-13144"},"PeriodicalIF":4.2000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoredox radical Truce–Smiles rearrangement of N-sulfinyl acrylamides with sulfoxonium ylides†\",\"authors\":\"Lin Tian , Pu Chen , Lindong Xiao , Huawen Huang\",\"doi\":\"10.1039/d5cc03513a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The visible light-induced Truce–Smiles rearrangement reaction of <em>N</em>-sulfinyl acrylamides with sulfoxonium ylides is herein reported. The reaction is performed under mild conditions by radical addition/aryl migration, allowing the synthesis of a range of valuable α-arylamides in moderate to good yields. The resultant α-aryl-γ-benzoylamides were converted by late-stage modification to a number of synthetically valuable derivatives.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 70\",\"pages\":\"Pages 13141-13144\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734525016921\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734525016921","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Photoredox radical Truce–Smiles rearrangement of N-sulfinyl acrylamides with sulfoxonium ylides†
The visible light-induced Truce–Smiles rearrangement reaction of N-sulfinyl acrylamides with sulfoxonium ylides is herein reported. The reaction is performed under mild conditions by radical addition/aryl migration, allowing the synthesis of a range of valuable α-arylamides in moderate to good yields. The resultant α-aryl-γ-benzoylamides were converted by late-stage modification to a number of synthetically valuable derivatives.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.