Phenolate anion-catalyzed direct activation of inert alkyl chlorides driven by visible light. Issue 22 (28th September 2021)

• Record Type: Journal Article
• Authors: Wei, Delian; Li, Xipan; Shen, Lei; Ding, Yuzhen; Liang, Kangjiang; Xia, Chengfeng
• Is Part Of: Organic chemistry frontiers. Volume 8:Issue 22(2021)
• Page Start: 6364
• Page End: 6370
• Publication Date: 2021-09-28
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/d1qo01128f
• Languages: English
• ISSNs: 2052-4110

Abstract

Abstract : A photochemical activation of inert alkyl chlorides catalyzed by phenolate anions was developed for C–O bond formation, dehalogenation, and cyclization under mild conditions. Abstract : Alkyl chlorides are abundant and stable chemical feedstocks, but their chemical inertness hinders their widespread availability as reactants in synthetic chemistry. In this study, we demonstrate an efficient photochemical strategy to activate inert C(sp 3 )–Cl bonds catalyzed by phenolate anion photocatalysts. Mechanistic studies indicate that the cleavage of unactivated C(sp 3 )–Cl bonds is mediated by a direct SET process from photo-excited phenolate anions. This strategy conveniently engages a diverse range of unactivated primary, secondary, and tertiary alkyl chlorides in radical C–O bond formation, dehalogenation, and cyclization under mild conditions.