Issue 18, 2022

Catalytic hydroaminations of alkynes: a facile protocol to vinyl-carbazole derivatives via a frustrated Lewis pair mechanism

Abstract

N-Vinylcarbazoles are important skeletons for photoluminescent materials. Herein, a transition metal-free, B(C6F5)3 mediated carbazolation reaction of alkynes is reported, providing 24 variants of N-vinylcarbazole derivatives. These N-vinylcarbazole products were obtained in good to excellent yields (up to 99%) under mild reaction conditions and could be performed on a gram scale.

Graphical abstract: Catalytic hydroaminations of alkynes: a facile protocol to vinyl-carbazole derivatives via a frustrated Lewis pair mechanism

Supplementary files

Article information

Article type
Communication
Submitted
21 Dec 2021
Accepted
07 Feb 2022
First published
07 Feb 2022

Chem. Commun., 2022,58, 3039-3042

Catalytic hydroaminations of alkynes: a facile protocol to vinyl-carbazole derivatives via a frustrated Lewis pair mechanism

Y. Zhao, L. Jin, J. Guo and D. W. Stephan, Chem. Commun., 2022, 58, 3039 DOI: 10.1039/D1CC07171H

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