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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Published Version: http://dx.doi.org/10.1016/j.tetlet.2005.12.084
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 |
|---|---|
| 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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