Issue 12, 2001

Molecular design of novel transition state analogues for molecular imprinting

Abstract

The synthesis and characterisation of novel polymerisable heterocycles containing boron is described. The compounds were designed to serve as transition state analogues of the enantioselective borane reduction of prochiral ketones with oxazaborolidine catalysts (CBS reduction). Preliminary results show that the heterocycles can be conveniently used as template monomers in the synthesis of molecularly imprinted polymers.

Article information

Article type
Paper
Submitted
16 Mar 2001
Accepted
15 Sep 2001
First published
21 Nov 2001

New J. Chem., 2001,25, 1537-1542

Molecular design of novel transition state analogues for molecular imprinting

A. Biffis and G. Wulff, New J. Chem., 2001, 25, 1537 DOI: 10.1039/B102500G

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