Issue 11, 2001
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

An efficient procedure for cleavage of aziridines with various thiols promoted by ZnCl2

Jie Wu,a   Xue-Long Hou*a  and  Li-Xin Daia  

* Corresponding authors

a State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai, China

Abstract

The ring-opening reaction of aziridines with various thiophenols and thiols catalyzed by ZnCl2 provides β-amino sulfides in high yield.

Graphical abstract: An efficient procedure for cleavage of aziridines with various thiols promoted by ZnCl2

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Article information

DOI
https://doi.org/10.1039/B100591J
Article type
Paper
Submitted
16 Jan 2001
Accepted
12 Apr 2001
First published
16 May 2001

J. Chem. Soc., Perkin Trans. 1, 2001, 1314-1317

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An efficient procedure for cleavage of aziridines with various thiols promoted by ZnCl2

J. Wu, X. Hou and L. Dai, J. Chem. Soc., Perkin Trans. 1, 2001, 1314 DOI: 10.1039/B100591J

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