| Literature DB >> 30702294 |
Hai-Yang Zhao1, Xing Gao1, Shu Zhang2, Xingang Zhang1.
Abstract
A nickel-catalyzed carbonylative difluoroalkylation reaction with arylboronic acids under 1 atm of CO has been developed. The reaction proceeds under mild reaction conditions with high efficiency and high functional group tolerance. Preliminary mechanistic studies reveal that the arylacyl nickel complex is the key intermediate to circumvent the formation of labile fluoroacyl nickel, and bimetallic oxidative addition is likely the key step to facilitate the catalytic cycle.Entities:
Year: 2019 PMID: 30702294 DOI: 10.1021/acs.orglett.8b04070
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005