Issue 87, 2022

Oxime ester-enabled anti-Markovnikov hydrosilylation of alkenes

Abstract

An oxime ester-enabled anti-Markovnikov hydrosilylation of alkenes is developed. This protocol is operationally simple and atom economical. The reaction shows broad functional group tolerance, such as ketones, amides, esters, epoxides, alcohols and carboxylic acids. Mono-substituted and geminally substituted alkenes could be chemoselectively hydrosilylated.

Graphical abstract: Oxime ester-enabled anti-Markovnikov hydrosilylation of alkenes

Supplementary files

Article information

Article type
Communication
Submitted
13 Jul 2022
Accepted
06 Oct 2022
First published
06 Oct 2022

Chem. Commun., 2022,58, 12204-12207

Oxime ester-enabled anti-Markovnikov hydrosilylation of alkenes

G. Shen, S. Fu and B. Liu, Chem. Commun., 2022, 58, 12204 DOI: 10.1039/D2CC03917F

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