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Enantioselective synthesis of the bicyclo[4.3.0]nonane ring system of the pinguisane-type sesquiterpenoids via a Br plain text. If you have a subtitle, it should be preceded with a colon [:]. Use capitals only for the first word and for proper nouns.

Clarke, P.A., Black, R.J.G. and Blake, A.J. (2006) Enantioselective synthesis of the bicyclo[4.3.0]nonane ring system of the pinguisane-type sesquiterpenoids via a Br plain text. If you have a subtitle, it should be preceded with a colon [:]. Use capitals only for the first word and for proper nouns. Tetrahedron Letters, 47 (9). pp. 1453-1455. ISSN 0040-4039

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Abstract

The bicyclo[4.3.0]nonane ring system of the pinguisane-type sesquiterpenoid natural products, including the vicinal quaternary stereocentres, has been synthesised as a single enantiomer via a novel Brønsted acid promoted transannular alkylation of an enol with an unactivated alkene.

Item Type: Article
Institution: The University of York
Academic Units: The University of York > Chemistry (York)
Depositing User: York RAE Import
Date Deposited: 11 Feb 2009 09:48
Last Modified: 11 Feb 2009 09:48
Published Version: http://dx.doi.org/10.1016/j.tetlet.2005.12.084
Status: Published
Publisher: Elsevier Science B.V., Amsterdam.
Identification Number: 10.1016/j.tetlet.2005.12.084
URI: http://eprints.whiterose.ac.uk/id/eprint/7590

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