Issue 7, 2005
From the journal:

Chemical Communications

NaI-catalyzed highly regioselective ring-opening [1 + 2] cycloaddition reaction of cyclopropenes with imines: highly stereoselective synthesis of cis-vinylic aziridines

Shengming Ma,*ab   Junliang Zhang,a   Lianghua Lu,a   Xin Jin,a   Yangjun Caib  and  Hairong Houa  

* Corresponding authors

a State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, P. R. China
E-mail: masm@mail.sioc.ac.cn
Fax: (+86)21-64167510

b Department of Chemistry, Zhejiang University, Hangzhou 310027, P. R. China

Abstract

cis-Vinylic aziridines were prepared highly stereoselectively via a NaI-catalyzed regioselective ring-opening [1 + 2] cycloaddition reaction of cyclopropenes with imines.

Graphical abstract: NaI-catalyzed highly regioselective ring-opening [1 + 2] cycloaddition reaction of cyclopropenes with imines: highly stereoselective synthesis of cis-vinylic aziridines

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B413807D
Article type
Communication
Submitted
07 Sep 2004
Accepted
16 Nov 2004
First published
05 Jan 2005

Chem. Commun., 2005, 909-911

Permissions

Request permissions

NaI-catalyzed highly regioselective ring-opening [1 + 2] cycloaddition reaction of cyclopropenes with imines: highly stereoselective synthesis of cis-vinylic aziridines

S. Ma, J. Zhang, L. Lu, X. Jin, Y. Cai and H. Hou, Chem. Commun., 2005, 909 DOI: 10.1039/B413807D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements