The University of Southampton
University of Southampton Institutional Repository

Zirconocene-Induced Cocyclisation/Elimination Reactions of 2-Heterosubstituted 1,6-Dienes and 1,6-Enynes

Zirconocene-Induced Cocyclisation/Elimination Reactions of 2-Heterosubstituted 1,6-Dienes and 1,6-Enynes
Zirconocene-Induced Cocyclisation/Elimination Reactions of 2-Heterosubstituted 1,6-Dienes and 1,6-Enynes
Zirconocene-mediated cocyclisation of 2-heterosubstituted-1,6-dienes and -enynes gave zirconacycles bearing an endocyclic beta-leaving group which eliminated under the reaction conditions to provide exocyclic alkylidene groups. The scope of this cyclisation/elimination has been investigated along with further elaboration of the monosubstituted zirconocene intermediates by insertion of alkenyl carbenoids.
zirconium, cyclisation, elimination, alkylidene, carbenoid insertion
0039-7881
2061-2074
Owen, David R.
e2cb2b65-7b58-446b-a329-2cff14ef84f9
Whitby, Richard J.
2e9f31e0-c2ed-49f2-9ee6-6eeb867575b3
Owen, David R.
e2cb2b65-7b58-446b-a329-2cff14ef84f9
Whitby, Richard J.
2e9f31e0-c2ed-49f2-9ee6-6eeb867575b3

Owen, David R. and Whitby, Richard J. (2005) Zirconocene-Induced Cocyclisation/Elimination Reactions of 2-Heterosubstituted 1,6-Dienes and 1,6-Enynes. Synthesis, 2061-2074. (doi:10.1055/s-2005-870029).

Record type: Article

Abstract

Zirconocene-mediated cocyclisation of 2-heterosubstituted-1,6-dienes and -enynes gave zirconacycles bearing an endocyclic beta-leaving group which eliminated under the reaction conditions to provide exocyclic alkylidene groups. The scope of this cyclisation/elimination has been investigated along with further elaboration of the monosubstituted zirconocene intermediates by insertion of alkenyl carbenoids.

This record has no associated files available for download.

More information

Published date: 1 August 2005
Keywords: zirconium, cyclisation, elimination, alkylidene, carbenoid insertion

Identifiers

Local EPrints ID: 20878
URI: http://eprints.soton.ac.uk/id/eprint/20878
ISSN: 0039-7881
PURE UUID: efa975f0-768f-4932-9346-f3347a76b907

Catalogue record

Date deposited: 31 Mar 2006
Last modified: 15 Mar 2024 06:26

Export record

Altmetrics

Contributors

Author: David R. Owen
Author: Richard J. Whitby

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×