{"title":"Rh(III)催化Csp2-H活化引发吲哚的2,3-二胺化反应","authors":"Chengjie Wang , Huanfeng Jiang , Wei Zeng","doi":"10.1039/d4qo02017k","DOIUrl":null,"url":null,"abstract":"<div><div>An Rh(<span>iii</span>)-catalyzed dearomative 2,3-diamination of indoles with <em>N</em>-alkoxyamides has been developed. The method provides an efficient approach to access 2-(<em>N</em>-acylimino)-3-aminoindolines with high regioselectivity.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 6","pages":"Pages 1821-1826"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dearomative 2,3-diamination of indoles triggered by Rh(iii)-catalyzed Csp2–H activation†\",\"authors\":\"Chengjie Wang , Huanfeng Jiang , Wei Zeng\",\"doi\":\"10.1039/d4qo02017k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>An Rh(<span>iii</span>)-catalyzed dearomative 2,3-diamination of indoles with <em>N</em>-alkoxyamides has been developed. The method provides an efficient approach to access 2-(<em>N</em>-acylimino)-3-aminoindolines with high regioselectivity.</div></div>\",\"PeriodicalId\":94379,\"journal\":{\"name\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"volume\":\"12 6\",\"pages\":\"Pages 1821-1826\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-22\",\"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/S2052412925000385\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","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/S2052412925000385","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Dearomative 2,3-diamination of indoles triggered by Rh(iii)-catalyzed Csp2–H activation†
An Rh(iii)-catalyzed dearomative 2,3-diamination of indoles with N-alkoxyamides has been developed. The method provides an efficient approach to access 2-(N-acylimino)-3-aminoindolines with high regioselectivity.