Issue 16, 2015

Palladium-catalyzed Hiyama coupling reaction of arylsulfonyl hydrazides under oxygen

Abstract

Palladium-catalyzed Hiyama cross-coupling reactions of various arylsulfonyl hydrazides with a wide variety of aryl silanes have been achieved in good to excellent yields under simple conditions. The newly developed catalytic system does not require the use of expensive silver- or copper-based stoichiometric oxidants and can be accelerated by the addition of TBAT under an atmosphere of oxygen. The reported Hiyama-type coupling reactions are tolerant to common functional groups, making these transformations attractive alternatives to the traditional cross-coupling approaches.

Graphical abstract: Palladium-catalyzed Hiyama coupling reaction of arylsulfonyl hydrazides under oxygen

Supplementary files

Article information

Article type
Communication
Submitted
23 Jan 2015
Accepted
10 Mar 2015
First published
18 Mar 2015

Org. Biomol. Chem., 2015,13, 4647-4651

Palladium-catalyzed Hiyama coupling reaction of arylsulfonyl hydrazides under oxygen

H. Miao, F. Wang, S. Zhou, G. Zhang and Y. Li, Org. Biomol. Chem., 2015, 13, 4647 DOI: 10.1039/C5OB00139K

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