Issue 10, 2022

A copper-catalyzed B–H bond insertion reaction of azide–ynamide with borane adducts via α-imino copper carbenes

Abstract

A new copper-catalyzed B–H bond insertion reaction between azide–ynamides and borane adducts has been developed, which represents the first B–H bond insertion into α-imino metal carbenes. This protocol enables the facile and practical synthesis of valuable organoborons in moderate to good yields with wide substrate scope and good functional group tolerance.

Graphical abstract: A copper-catalyzed B–H bond insertion reaction of azide–ynamide with borane adducts via α-imino copper carbenes

Supplementary files

Article information

Article type
Research Article
Submitted
21 Mar 2022
Accepted
10 Apr 2022
First published
12 Apr 2022

Org. Chem. Front., 2022,9, 2773-2778

A copper-catalyzed B–H bond insertion reaction of azide–ynamide with borane adducts via α-imino copper carbenes

C. Weng, G. Zhu, B. Zhu, P. Qian, X. Zhu, J. Zhou and L. Ye, Org. Chem. Front., 2022, 9, 2773 DOI: 10.1039/D2QO00457G

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