{"title":"Rh(III)-Catalyzed Imidoyl C-H Bond Activation/[4 + 2] Annulation of N-Benzimidazole Imines with Iodonium Ylides.","authors":"Xiang Li,Qin Zhang,Xin Zheng","doi":"10.1021/acs.joc.5c01368","DOIUrl":null,"url":null,"abstract":"A general protocol for the synthesis of polycyclic benzo[4,5]imidazo[1,2-a]pyrimidines via Rh(III)-catalyzed imidoyl C-H bond activation of N-benzimidazole imines with iodonium ylides has been disclosed. This method features mild conditions, a broad substrate scope, and excellent functional group tolerance. Moreover, the reaction could be easily scaled up and was amendable with the in situ generated iodonium ylides, which demonstrated the practicality of this method.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"108 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.5c01368","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
A general protocol for the synthesis of polycyclic benzo[4,5]imidazo[1,2-a]pyrimidines via Rh(III)-catalyzed imidoyl C-H bond activation of N-benzimidazole imines with iodonium ylides has been disclosed. This method features mild conditions, a broad substrate scope, and excellent functional group tolerance. Moreover, the reaction could be easily scaled up and was amendable with the in situ generated iodonium ylides, which demonstrated the practicality of this method.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.