Issue 11, 2017

Catalytic and catalyst-free diboration of alkynes

Abstract

The diboration of alkynes has become the most straightforward and powerful method for the synthesis of functionalized 1,2-diborylalkenes, which are widely used as building blocks in organic synthesis. The present review provides a comprehensive summary of the diboration of alkynes, including platinum-, palladium-, cobalt-, copper-, iridium-, gold-, iron-, base- and small organic molecule-catalyzed diboration, direct and metal-free diboration, and base-promoted diboration of alkynes up to early 2017. The reaction conditions, regio- and stereoselectivities, and mechanisms are summarized in detail. Moreover, synthetic applications and perspectives on the diboration of alkynes are also discussed.

Graphical abstract: Catalytic and catalyst-free diboration of alkynes

Article information

Article type
Review Article
Submitted
21 Jul 2017
Accepted
28 Aug 2017
First published
05 Sep 2017

Org. Chem. Front., 2017,4, 2235-2255

Catalytic and catalyst-free diboration of alkynes

F. Zhao, X. Jia, P. Li, J. Zhao, Y. Zhou, J. Wang and H. Liu, Org. Chem. Front., 2017, 4, 2235 DOI: 10.1039/C7QO00614D

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