| Literature DB >> 34422448 |
Nikita Kvasovs1, Valeriia Iziumchenko1, Vitalii Palchykov1, Vladimir Gevorgyan1.
Abstract
A visible light-induced palladium-catalyzed oxidative C-H alkylation of oximes has been developed. This mild protocol allows for an efficient atom economical C-C bond construction of alkyl-substituted oximes. A broad range of primary, secondary, and tertiary alkyl bromides and iodides, as well as a range of different formaldoximes, can efficiently undergo this transformation. The method features visible light-induced generation of nucleophilic hybrid alkyl Pd radical intermediates, which upon radical addition at the imine moiety and a subsequent β-hydrogen elimination deliver substituted imines.Entities:
Keywords: Heck reaction; alkylation; light-induced; oxime; palladium; radical
Year: 2021 PMID: 34422448 PMCID: PMC8372551 DOI: 10.1021/acscatal.1c00267
Source DB: PubMed Journal: ACS Catal Impact factor: 13.084