Issue 4, 2016

Synthesis of 1,1-diboronate esters by cobalt-catalyzed sequential hydroboration of terminal alkynes

Abstract

A cobalt complex of iminopyridine-oxazoline catalyzes sequential hydroboration of alkyl and aryl alkynes with pinacolborane to form 1,1-diboronate esters. The reactions proceed under mild conditions with high yields, high regioselectivity, and wide functional group tolerance. The synthetic utility of 1,1-di(boronates) is demonstrated by chemoselective monoarylation and stepwise diarylation through palladium-catalyzed Suzuki–Miyaura coupling reactions.

Graphical abstract: Synthesis of 1,1-diboronate esters by cobalt-catalyzed sequential hydroboration of terminal alkynes

Supplementary files

Article information

Article type
Research Article
Submitted
04 ربيع الأول 1437
Accepted
14 ربيع الثاني 1437
First published
16 ربيع الثاني 1437
This article is Open Access
Creative Commons BY license

Org. Chem. Front., 2016,3, 434-438

Synthesis of 1,1-diboronate esters by cobalt-catalyzed sequential hydroboration of terminal alkynes

Z. Zuo and Z. Huang, Org. Chem. Front., 2016, 3, 434 DOI: 10.1039/C5QO00426H

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