Issue 21, 2016

Gold/gallium-catalyzed annulation of 1,3-dicarbonyl compounds and cyclopropylacetylenes for synthesis of substituted cyclopentenes

Abstract

An efficient synthesis of substituted cyclopentenes through gold/gallium-catalyzed annulation of 1,3-dicarbonyl compounds and cyclopropylacetylenes is achieved. This tandem reaction consists of a gold-catalyzed Nakamura reaction, a catalytic dienol–enone tautomerization, and a gallium-catalyzed vinylcyclopropane (VCP) rearrangement.

Graphical abstract: Gold/gallium-catalyzed annulation of 1,3-dicarbonyl compounds and cyclopropylacetylenes for synthesis of substituted cyclopentenes

Supplementary files

Article information

Article type
Communication
Submitted
11 Jan 2016
Accepted
03 Feb 2016
First published
04 Feb 2016

RSC Adv., 2016,6, 17386-17389

Author version available

Gold/gallium-catalyzed annulation of 1,3-dicarbonyl compounds and cyclopropylacetylenes for synthesis of substituted cyclopentenes

B. Dong, Y. Xi, Y. Su, N. G. Akhmedov, J. L. Petersen and X. Shi, RSC Adv., 2016, 6, 17386 DOI: 10.1039/C6RA00896H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements