Srikrishna, A and Anebouselvy, K (2002) An enantiospecific approach to (+)-thaps-8(11)-en-3-ol. In: Tetrahedron Letters, 43 (15). pp. 2769-2771.
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Abstract
An enantiospecific synthesis of a thapsane containing an oxygen substituent at the C-3 position is accomplished starting from (R)-carvone. A Claisen rearrangement and an intramolecular diazoketone cyclopropanation reaction were employed for the stereo- and regiospecific generation of the three contiguous quaternary carbon atoms present in the thapsanes.
| Item Type: | Journal Article |
|---|---|
| Additional Information: | Copyright of this article belongs to Elsevier Science Ltd. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 03 Oct 2007 |
| Last Modified: | 19 Sep 2010 04:39 |
| URI: | http://eprints.iisc.ernet.in/id/eprint/12006 |
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