| Literature DB >> 28717256 |
Lei Han1, Jibao Xia1, Lin You1, Chuo Chen1.
Abstract
Photoexcited arylketones catalyze the direct chlorination of C(sp3)-H groups by N-chlorosuccinimide. Acetophenone is the most effective catalyst for functionalization of unactivated C-H groups while benzophenone provides better yields for benzylic C-H functionalization. Activation of both acetophenone and benzophenone can be achieved by irradiation with a household compact fluorescent lamp. This light-dependent reaction provides a better control of the reaction as compared to the traditional chlorination methods that proceed through a free radical chain propagation mechanism.Entities:
Keywords: Arylketone; Chlorination; C–H functionalization; Photochemistry; Visible light
Year: 2017 PMID: 28717256 PMCID: PMC5510956 DOI: 10.1016/j.tet.2017.05.008
Source DB: PubMed Journal: Tetrahedron ISSN: 0040-4020 Impact factor: 2.457