Issue 10, 2006
From the journal:

Chemical Communications

Sequential ring closing/opening metathesis for the highly selective synthesis of a triply bifunctionalized α-cyclodextrin†

Olivia Bistri,a   Pierre Sinaÿa  and  Matthieu Sollogoub*a  

* Corresponding authors

a Ecole Normale Supérieure, Département de Chimie, Institut de chimie moléculaire (FR 2769), UMR 8642: CNRS-ENS-UPMC Paris 6, 24 rue Lhomond, Paris Cedex 05, Paris, France
E-mail: sollo@ens.fr
Fax: 33 144323397
Tel: 33 144323335

Abstract

Metathesis versatility has been exploited to reveal the cyclic directionality of cyclodextrins and to selectively synthesise a unique cyclodextrin bearing three pairs of orthogonal protecting groups on its primary rim.

Graphical abstract: Sequential ring closing/opening metathesis for the highly selective synthesis of a triply bifunctionalized α-cyclodextrin

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B510329K
Article type
Communication
Submitted
21 Jul 2005
Accepted
22 Nov 2005
First published
12 Dec 2005

Chem. Commun., 2006, 1112-1114

Permissions

Request permissions

Sequential ring closing/opening metathesis for the highly selective synthesis of a triply bifunctionalized α-cyclodextrin

O. Bistri, P. Sinaÿ and M. Sollogoub, Chem. Commun., 2006, 1112 DOI: 10.1039/B510329K

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