| Literature DB >> 26461434 |
Yu-Tao He1, Qiang Wang1, Lian-Hua Li1, Xue-Yuan Liu1, Peng-Fei Xu1, Yong-Min Liang1,2.
Abstract
A palladium-catalyzed aryldifluoroalkylation of alkynes with ethyl difluoroiodoacetate and arylboronic acids as reaction partners is described. The alkyne difunctionalization process provides various aryldifluoroalkylated products in one pot under mild reaction conditions. A wide range of alkynes and diverse arylboronic acids are compatible with these reaction conditions. High reaction efficiency and broad substrate scope are the notable features of this transformation. Preliminary mechanistic investigations indicate that a difluoroalkyl radical addition pathway is involved in this transformation.Entities:
Year: 2015 PMID: 26461434 DOI: 10.1021/acs.orglett.5b02512
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005