| Literature DB >> 32356425 |
Liyan Feng1, Lin Guo1, Chao Yang1, Jia Zhou1, Wujiong Xia1.
Abstract
A palladium-catalyzed Narasaka-Heck reaction by a domino cross-coupling reaction with aromatic alkenes under blue LED irradiation at room temperature was developed. The undesired β-hydride elimination of the hybrid alkyl palladium radical species was prohibited, enabling a broad range of oxime esters to undergo 5-exo cyclization and subsequent coupling with olefins. The practicality of the method was well illustrated by the construction of a nitrogen bridgehead tricycle as a core skeleton of alkaloids.Entities:
Year: 2020 PMID: 32356425 DOI: 10.1021/acs.orglett.0c01267
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005