Uncovering the Reactivity of Direct Photoredox Catalyzed α-C–H Alkylation of Alcohols: A Boron-Free Procedure

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Authors: Geneviève O’Keefe, Dennis G. Hall
Cited by: 2
References: 28

Abstract

Alcohol functionalization is an important class of pharmaceutically relevant transformations that have increasingly been achieved through photoredox-hydrogen atom transfer catalysis. Many methods rely on exogenous bond-weakening activators such as boron-based catalysts. Herein, a reported hemiboronic acid catalyst was shown to dynamically interact with alcohols, however, with no effect on the efficiency or stereoselectivity of the α-C-H alkylation of alcohols. A simplified procedure affords products in yields of 18-95% without a boron cocatalyst.

Fields of Study & Subjects

Organoboron and organosilicon chemistry Catalytic C–H Functionalization Methods Radical Photochemical Reactions

Publication details

Journal / source
Organic Letters
Publisher
American Chemical Society (ACS)
Volume
28
Issue
9
Pages
2985–2989
Publication date
24 February 2026
Language
EN