Jump to main content
Jump to site search

Issue 46, 2013
Previous Article Next Article

Palladium-catalyzed Suzuki cross-coupling of N′-tosyl arylhydrazines

Author affiliations

Abstract

The first palladium-catalyzed Suzuki cross-coupling of N′-tosyl arylhydrazines with various organoboron reagents has been developed for the preparation of biaryl compounds in high yields. N′-Tosyl arylhydrazine as a readily available and stable electrophile also demonstrated its generality in a number of coupling reactions.

Graphical abstract: Palladium-catalyzed Suzuki cross-coupling of N′-tosyl arylhydrazines

Back to tab navigation

Supplementary files

Article information


Submitted
24 Feb 2013
Accepted
15 Apr 2013
First published
19 Apr 2013

Chem. Commun., 2013,49, 5268-5270
Article type
Communication

Palladium-catalyzed Suzuki cross-coupling of N′-tosyl arylhydrazines

J. Liu, H. Yan, H. Chen, Y. Luo, J. Weng and G. Lu, Chem. Commun., 2013, 49, 5268
DOI: 10.1039/C3CC41421C

Social activity

Search articles by author

Spotlight

Advertisements