Access to α-Hydroxy Amides via a Practical Metal-Free "One-Pot" Tandem Reaction Involving Aerobic C(sp3)-H Hydroxylation and C(sp2)-C(sp3) Cleavage

J Org Chem. 2022 Dec 16;87(24):16263-16275. doi: 10.1021/acs.joc.2c01839. Epub 2022 Dec 5.

Abstract

A flexible metal-free cascade reaction involving aerobic C(sp3)-H hydroxylation and decarbonylation with high regioselectivity and functional group tolerance has been established. Moreover, this indirect hydroxylation approach of N-aryl amides could enable the construction of a wide range of valuable secondary alcohols at α-position of N-aryl amides. It provides a supplementary strategy for direct α-hydroxylation of simple amides.