Issue 38, 2013
From the journal:

RSC Advances

Organocatalyzed aza-Michael–Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers†

You-ming Huang,a   Chang-wu Zhenga  and  Gang Zhao*a  

* Corresponding authors

a Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China
E-mail: zhaog@mail.sioc.ac.cn

Abstract

An efficient organocatalytic aza-Michael–Michael cascade reaction for the asymmetric synthesis of highly functionalized spirooxindole tetrahydroquinolines has been reported through a formal [4+2] annulation strategy.

Graphical abstract: Organocatalyzed aza-Michael–Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C3RA42783H
Article type
Communication
Submitted
05 Jun 2013
Accepted
25 Jul 2013
First published
26 Jul 2013

RSC Adv., 2013,3, 16999-17002

Permissions

Request permissions

Organocatalyzed aza-Michael–Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers

Y. Huang, C. Zheng and G. Zhao, RSC Adv., 2013, 3, 16999 DOI: 10.1039/C3RA42783H

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