Issue 39, 2009
From the journal:

Chemical Communications

Highly enantioselective intramolecular Michael reactions by d-camphor-derived triazolium salts†

Yi Li,a   Xue-Qiang Wang,a   Chao Zhenga  and  Shu-Li You*a  

* Corresponding authors

a State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Linglin Lu, Shanghai 200032, P. R. China
E-mail: slyou@mail.sioc.ac.cn
Fax: (+86) 21-54925087

Abstract

Camphor-derived chiral triazolium salts have been found to be highly efficient for asymmetric intramolecular Michael reactions. With 1–5 mol% of the catalyst, the desired products were obtained in excellent yields, with up to 99% ee.

Graphical abstract: Highly enantioselective intramolecular Michael reactions by d-camphor-derived triazolium salts

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B914805A
Article type
Communication
Submitted
22 Jul 2009
Accepted
22 Aug 2009
First published
08 Sep 2009

Chem. Commun., 2009, 5823-5825

Permissions

Request permissions

Highly enantioselective intramolecular Michael reactions by D-camphor-derived triazolium salts

Y. Li, X. Wang, C. Zheng and S. You, Chem. Commun., 2009, 5823 DOI: 10.1039/B914805A

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