Issue 35, 2006
From the journal:

Chemical Communications

Surfactant-type asymmetric organocatalyst: organocatalytic asymmetric Michael addition to nitrostyrenes in water†

Sanzhong Luo,*a   Xueling Mi,b   Song Liu,b   Hui Xua  and  Jin-Pei Cheng*ab  

* Corresponding authors

a Beijing National Laboratory for Molecular Sciences (BNLMS), Centre for Molecular Science, Institute of Chemistry, Chinese Academy of Science, Beijing, China
E-mail: luosz@iccas.ac.cn
Fax: +86-10-62554449
Tel: +86-1062554446

b Department of Chemistry and State-key Laboratory of Elemento-organic Chemistry, Nankai University, Tianjin, China
E-mail: chengjp@mail.most.gov.cn

Abstract

A surfactant-type asymmetric organocatalyst (STAO) catalyzed highly efficient Michael addition to nitroalkenes with high stereoselectivities in water without using any organic solvents or additional additives.

Graphical abstract: Surfactant-type asymmetric organocatalyst: organocatalytic asymmetric Michael addition to nitrostyrenes in water

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Article information

DOI
https://doi.org/10.1039/B607846J
Article type
Communication
Submitted
02 Jun 2006
Accepted
03 Jul 2006
First published
28 Jul 2006

Chem. Commun., 2006, 3687-3689

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Surfactant-type asymmetric organocatalyst: organocatalytic asymmetric Michael addition to nitrostyrenes in water

S. Luo, X. Mi, S. Liu, H. Xu and J. Cheng, Chem. Commun., 2006, 3687 DOI: 10.1039/B607846J

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