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
2061-2074
Owen, David R.
e2cb2b65-7b58-446b-a329-2cff14ef84f9
Whitby, Richard J.
2e9f31e0-c2ed-49f2-9ee6-6eeb867575b3
1 August 2005
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, .
(doi:10.1055/s-2005-870029).
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.
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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
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Date deposited: 31 Mar 2006
Last modified: 15 Mar 2024 06:26
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Author:
David R. Owen
Author:
Richard J. Whitby
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