Issue 7, 2016

Cobalt(iii)-catalyzed efficient synthesis of indenones through carboannulation of benzoates and alkynes

Abstract

Cobalt(III)-catalyzed C–H activation of simple benzoate esters has been achieved, and redox-neutral annulative coupling with internal alkynes allowed efficient synthesis of indenones. The employment of the weak and simple ester directing group makes it an attractive protocol in carbocycle synthesis.

Graphical abstract: Cobalt(iii)-catalyzed efficient synthesis of indenones through carboannulation of benzoates and alkynes

Supplementary files

Article information

Article type
Research Article
Submitted
31 Mar 2016
Accepted
27 Apr 2016
First published
28 Apr 2016

Org. Chem. Front., 2016,3, 813-816

Cobalt(III)-catalyzed efficient synthesis of indenones through carboannulation of benzoates and alkynes

L. Kong, X. Yang, X. Zhou, S. Yu and X. Li, Org. Chem. Front., 2016, 3, 813 DOI: 10.1039/C6QO00134C

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