Issue 12, 2008
From the journal:

Organic & Biomolecular Chemistry

A simple, efficient Pd-catalyzed synthesis of N-sulfonylimines from organoboronic acids and tosylbenzimidoyl chlorides†

Li-Yan Fan,b   Fei-Feng Gao,a   Wei-Hua Jiang,a   Min-Zhi Deng*a  and  Chang-Tao Qian*a  

* Corresponding authors

a State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China
E-mail: qianct@mail.sioc.ac.cn
Fax: +86 21-64166128

b Visiting Scholar from: Department of Chemistry, Tongji University, Shanghai, China
E-mail: fanly@mail.tongji.edu.cn

Abstract

A simple and efficient synthesis of N-sulfonyl ketimines through a Pd-catalyzed cross-coupling reaction between organoboronic acids and tosylbenzimidoyl chlorides under mild conditions has been developed.

Graphical abstract: A simple, efficient Pd-catalyzed synthesis of N-sulfonylimines from organoboronic acids and tosylbenzimidoyl chlorides

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Article information

DOI
https://doi.org/10.1039/B802867B
Article type
Paper
Submitted
19 Feb 2008
Accepted
11 Mar 2008
First published
11 Apr 2008

Org. Biomol. Chem., 2008,6, 2133-2137

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A simple, efficient Pd-catalyzed synthesis of N-sulfonylimines from organoboronic acids and tosylbenzimidoyl chlorides

L. Fan, F. Gao, W. Jiang, M. Deng and C. Qian, Org. Biomol. Chem., 2008, 6, 2133 DOI: 10.1039/B802867B

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