| Literature DB >> 32315187 |
Xuewen Yi1,2, Siyu Lei1, Wangsheng Liu2, Fengrui Che1, Chunzheng Yu1, Xuesong Liu1, Zonghua Wang1, Xin Zhou1, Yuexia Zhang1.
Abstract
An unprecedented N-demethylation of N-methyl amides has been developed by use of N-fluorobenzenesulfonimide as an oxidant with the aid of a copper catalyst. The conversion of amides to carbinolamines involves successive single-electron transfer, hydrogen-atom transfer, and hydrolysis, and is accompanied by formation of N-(phenylsulfonyl)benzenesulfonamide. Carbinolamines spontaneously decompose to N-demethylated amides and formaldehyde, because of their inherent instability.Entities:
Year: 2020 PMID: 32315187 DOI: 10.1021/acs.orglett.0c00863
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005