Issue 28, 2016

Cp*Rh(iii)-catalyzed electrophilic amination of arylboronic acids with azo compounds for synthesis of arylhydrazides

Abstract

A [Cp*Rh(III)]-catalyzed electrophilic amination of arylboronic acids with diethyl azodicarboxylate (DEAD) was developed, and arylhydrazides were produced in excellent yields and selectivity. The analogous amination with the arylazocarboxylates afforded the corresponding N,N-diarylhydrazides. The electrophilic amination of arylboronic acids with azocarboxylates proceeds readily under mild conditions with excellent functional group tolerance. Up to 99% yields were obtained. Preliminary mechanistic studies revealed that prior formation of an arylrhodium(III) intermediate for the azo coupling reaction can be ruled out.

Graphical abstract: Cp*Rh(iii)-catalyzed electrophilic amination of arylboronic acids with azo compounds for synthesis of arylhydrazides

Supplementary files

Article information

Article type
Paper
Submitted
06 Apr 2016
Accepted
14 Jun 2016
First published
16 Jun 2016
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2016,14, 6821-6825

Cp*Rh(III)-catalyzed electrophilic amination of arylboronic acids with azo compounds for synthesis of arylhydrazides

Y. Lau, C. Chan, Z. Zhou and W. Yu, Org. Biomol. Chem., 2016, 14, 6821 DOI: 10.1039/C6OB00719H

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