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

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.

DOI: 10.1039/b802867b

Cite this paper

@article{Fan2008ASE, title={A simple, efficient Pd-catalyzed synthesis of N-sulfonylimines from organoboronic acids and tosylbenzimidoyl chlorides.}, author={L Fan and Fei-Feng Gao and Wei-Hua Jiang and Min-zhi Deng and Chang-Tao Qian}, journal={Organic & biomolecular chemistry}, year={2008}, volume={6 12}, pages={2133-7} }