Issue 2, 2006
From the journal:

Chemical Communications

Protonated N′-benzyl-N′-prolyl proline hydrazide as highly enantioselective catalyst for direct asymmetric aldol reaction†

Chuanling Cheng,ade   Jian Sun,*a   Chao Wang,ae   Yu Zhang,ae   Siyu Wei,a   Fan Jiangb  and  Yundong Wu*bc  

* Corresponding authors

a Chengdu Institute of Biology, Chinese Academy of Sciences, China
E-mail: sunjian@cib.ac.cn
Fax: +86-28-85222753
Tel: +86-28-85211220

b College of Chemistry, Peking University, China

c Department of chemistry, The Hong Kong University of Science and Technology, Kowloon, Hong Kong, China

d Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu

e Graduate School of Chinese Academy of Sciences, Beijing, China

Abstract

Protonated N′-benzyl-N′-L-prolyl-L-proline hydrazide has been developed as a highly enantioselective catalyst for the asymmetric direct aldol reaction of aromatic aldehydes with ketones.

Graphical abstract: Protonated N′-benzyl-N′-prolyl proline hydrazide as highly enantioselective catalyst for direct asymmetric aldol reaction

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B511992H
Article type
Communication
Submitted
24 ago. 2005
Accepted
18 oct. 2005
First published
18 nov. 2005

Chem. Commun., 2006, 215-217

Permissions

Request permissions

Protonated N′-benzyl-N′-prolyl proline hydrazide as highly enantioselective catalyst for direct asymmetric aldol reaction

C. Cheng, J. Sun, C. Wang, Y. Zhang, S. Wei, F. Jiang and Y. Wu, Chem. Commun., 2006, 215 DOI: 10.1039/B511992H

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