Issue 73, 2013

Exploiting dense shell/packing principles to invoke stereoselectivity in a reaction accelerated by a chiral dendrimer

Abstract

As dendrimers approach their dense shell or dense packed limit, a certain amount of conformational organization exists. Any substrate binding within the dendrimer's external layer will experience the same organizational effects. This paper describes how these effects can be exploited towards stereocontrol with respect to binding and reactivity.

Graphical abstract: Exploiting dense shell/packing principles to invoke stereoselectivity in a reaction accelerated by a chiral dendrimer

Supplementary files

Article information

Article type
Communication
Submitted
21 May 2013
Accepted
24 Jul 2013
First published
25 Jul 2013
This article is Open Access
Creative Commons BY license

Chem. Commun., 2013,49, 8063-8065

Exploiting dense shell/packing principles to invoke stereoselectivity in a reaction accelerated by a chiral dendrimer

A. Ellis, M. Wallace and L. J. Twyman, Chem. Commun., 2013, 49, 8063 DOI: 10.1039/C3CC43830A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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