Issue 24, 2001
From the journal:

Chemical Communications

The enantioselective generation of bridgehead enolates

Alexander J. Blake,a   Gerard M. P. Giblin,b   Douglas T. Kirk,a   Nigel S. Simpkins*a  and  Claire Wilsona  

* Corresponding authors

a School of Chemistry, The University of Nottingham, University Park, Nottingham, UK
E-mail: Nigel.Simpkins@Nottingham.ac.uk;
Fax: +44(0) 115 951 3564;
Tel: +44(0) 115 951 3533

b GlaxoSmithKline, Medicines Research Centre, Gunnels Wood Road, Hertfordshire, Stevenage, UK

Abstract

The generation and silylation of bridgehead enolates has been accomplished in high enantiomeric excess using a chiral lithium amide base.

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B108986M
Article type
Communication
Submitted
03 Oct 2001
Accepted
12 Nov 2001
First published
06 Dec 2001

Chem. Commun., 2001, 2668-2669

Permissions

Request permissions

The enantioselective generation of bridgehead enolates

A. J. Blake, G. M. P. Giblin, D. T. Kirk, N. S. Simpkins and C. Wilson, Chem. Commun., 2001, 2668 DOI: 10.1039/B108986M

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