Issue 48, 2010
From the journal:

Chemical Communications

Enantioselective heterocyclic synthesis of spiro chromanone–thiochroman complexes catalyzed by a bifunctional indane catalyst†

Yaojun Gao,a   Qiao Ren,a   Hao Wu,a   Maoguo Lia  and  Jian Wang*a  

* Corresponding authors

a Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543
E-mail: chmwangj@nus.edu.sg
Fax: (+) 65-6516-1691

Abstract

Novel asymmetric domino reactions of benzylidenechroman-4-ones and 2-mercaptobenzaldehydes for efficient construction of spiro chromanone–thiochroman complexes were accomplished with high yields and excellent selectivities via a novel bifunctional indane catalyst.

Graphical abstract: Enantioselective heterocyclic synthesis of spiro chromanone–thiochroman complexes catalyzed by a bifunctional indane catalyst

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C0CC03489D
Article type
Communication
Submitted
26 Aug 2010
Accepted
07 Oct 2010
First published
04 Nov 2010

Chem. Commun., 2010,46, 9232-9234

Permissions

Request permissions

Enantioselective heterocyclic synthesis of spiro chromanone–thiochroman complexes catalyzed by a bifunctional indane catalyst

Y. Gao, Q. Ren, H. Wu, M. Li and J. Wang, Chem. Commun., 2010, 46, 9232 DOI: 10.1039/C0CC03489D

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