Bis(N-heterocyclic carbene)-Borylene-Mediated Heteroallene Activation

Abstract

This study describes a bis(N-heterocyclic carbene)-borylene that activates heteroallenes. The borylene undergoes Staudinger reaction with azide to afford an NHC-iminoborane, and it also catalyzes the cyclotrimerization of isocyanates to give isocyanurates. In the presence of excess pinacolborane, it catalyzes the chemoselective hydroboration of isocyanates to form N-boryl formamides.

Supplementary files

Article information

Article type
Communication
Submitted
08 Jan 2026
Accepted
11 Feb 2026
First published
17 Feb 2026
This article is Open Access
Creative Commons BY license

Chem. Commun., 2026, Accepted Manuscript

Bis(N-heterocyclic carbene)-Borylene-Mediated Heteroallene Activation

A. Koh, G. Vernezoul, J. Fan, Z. Zhang, M. Su and C. So, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC00146G

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