Issue 12, 2021

Theoretical evaluation of the carbene-based site-selectivity in gold(iii)-catalyzed annulations of alkynes with anthranils

Abstract

The gold(III)-catalyzed annulations of alkynes with anthranils were evaluated using DFT calculations. A unified rationale for the Br-migration on α-imino gold(III)-carbene was proposed, from which an unprecedented “N-donation/abstraction substitution” mechanism was established using the substituted anthranils, while direct C–H nucleophilic attack was involved with the unsubstituted anthranils. The controlling factors guiding the site-selectivity were uncovered. These computational studies provide insight for developing new α-imino gold(III)-carbene mediated reactions.

Graphical abstract: Theoretical evaluation of the carbene-based site-selectivity in gold(iii)-catalyzed annulations of alkynes with anthranils

Supplementary files

Article information

Article type
Communication
Submitted
12 Nov 2020
Accepted
23 Dec 2020
First published
23 Dec 2020
This article is Open Access
Creative Commons BY license

Chem. Commun., 2021,57, 1494-1497

Theoretical evaluation of the carbene-based site-selectivity in gold(III)-catalyzed annulations of alkynes with anthranils

K. Wang, Q. Wu, S. Bi, L. Liu, G. Chen, Y. Li, T. D. James and Y. Liu, Chem. Commun., 2021, 57, 1494 DOI: 10.1039/D0CC07440C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements