{"title":"可见光诱导吖啶催化的n -杂环选择性脱烷基反应","authors":"Shanshan Liu , Yaoyao Zhang , Xianying Zhou , Lin-Yu Jiao","doi":"10.1039/d5cc00609k","DOIUrl":null,"url":null,"abstract":"<div><div>We have developed an efficient and general strategy for <em>N</em>-chlorosuccinimide (NCS)-promoted <em>N</em>-dealkylation of aza-heterocycles <em>via</em> acridinium-photocatalyzed electron transfer and hydrogen atom transfer. This approach effectively obviates the need for transition metal catalysis and features wide substrate scope as well as exclusive chemo-selectivity. Remarkably, the method allowed the deprotection of the privileged but stable <em>N</em>-alkyl group, thus filling a gap in the practical <em>N</em>-dealkylation of N-heteroaromatics.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 41","pages":"Pages 7450-7453"},"PeriodicalIF":4.3000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible-light-induced acridinium-catalyzed selective N-dealkylation of N-heterocycles†\",\"authors\":\"Shanshan Liu , Yaoyao Zhang , Xianying Zhou , Lin-Yu Jiao\",\"doi\":\"10.1039/d5cc00609k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>We have developed an efficient and general strategy for <em>N</em>-chlorosuccinimide (NCS)-promoted <em>N</em>-dealkylation of aza-heterocycles <em>via</em> acridinium-photocatalyzed electron transfer and hydrogen atom transfer. This approach effectively obviates the need for transition metal catalysis and features wide substrate scope as well as exclusive chemo-selectivity. Remarkably, the method allowed the deprotection of the privileged but stable <em>N</em>-alkyl group, thus filling a gap in the practical <em>N</em>-dealkylation of N-heteroaromatics.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 41\",\"pages\":\"Pages 7450-7453\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-04-23\",\"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/S1359734525008110\",\"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/S1359734525008110","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Visible-light-induced acridinium-catalyzed selective N-dealkylation of N-heterocycles†
We have developed an efficient and general strategy for N-chlorosuccinimide (NCS)-promoted N-dealkylation of aza-heterocycles via acridinium-photocatalyzed electron transfer and hydrogen atom transfer. This approach effectively obviates the need for transition metal catalysis and features wide substrate scope as well as exclusive chemo-selectivity. Remarkably, the method allowed the deprotection of the privileged but stable N-alkyl group, thus filling a gap in the practical N-dealkylation of N-heteroaromatics.
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.