Srikrishna, A and Pardeshi, Vijendra H and Satyanarayana, G (2007) A rapid enantiospecific synthesis of the (6,6,5)-tricyclic ring system of the elisabethane diterpenes. In: Tetrahedron Letters, 48 (23). pp. 4087-4090.
PDF
665.pdf Restricted to Registered users only Download (130kB) | Request a copy |
Abstract
A rapid enantiospecific stereoselective synthesis of the 6,6,5-ring system of the novel tricyclic elisabethin diterpenes, starting from (R)-carvone, employing a ROM-RCM sequence as the key step, has been accomplished.
Item Type: | Journal Article |
---|---|
Publication: | Tetrahedron Letters |
Publisher: | Elsevier |
Additional Information: | Copyright of this article belongs to Elsevier. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 03 Jul 2008 |
Last Modified: | 19 Sep 2010 04:46 |
URI: | http://eprints.iisc.ac.in/id/eprint/14721 |
Actions (login required)
View Item |