Issue 6, 2019

Annulating thiazolium cations via a direct double C–H activation strategy: Rh–N,S-heterocyclic carbene is the key

Abstract

Herein we show how metal–N,S-heterocyclic carbene intermediates are conveniently generated and utilized for the first time to construct N,S doubly-doped cationic conjugated tricyclic organic molecules which exhibit tuneable emission. The chemistry proceeds via direct double C–H activation followed by an annulative π-extension pathway.

Graphical abstract: Annulating thiazolium cations via a direct double C–H activation strategy: Rh–N,S-heterocyclic carbene is the key

Supplementary files

Article information

Article type
Communication
Submitted
17 Sep 2018
Accepted
14 Dec 2018
First published
14 Dec 2018

Chem. Commun., 2019,55, 854-857

Annulating thiazolium cations via a direct double C–H activation strategy: Rh–N,S-heterocyclic carbene is the key

C. Dutta, A. B. Sainaba and J. Choudhury, Chem. Commun., 2019, 55, 854 DOI: 10.1039/C8CC07531J

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