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A general, ring closure metathesis based enantiospecific approach to polyfunctional eudesmane, eremophilane and agarofuran sesquiterpenoids

Mehta, Goverdhan and Kumaran, Senthil R (2003) A general, ring closure metathesis based enantiospecific approach to polyfunctional eudesmane, eremophilane and agarofuran sesquiterpenoids. In: Tetrahedron Letters, 44 (37). pp. 7055-7059.

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Abstract

An enantiospecific and stereo- and functional group diversity oriented approach to eudesmane, eremophilane and agarofuran sesquiterpenoids from (−)-carvone has been devised. RCM has been employed as the key reaction to generate the highly functionalized eudesmane framework. Further elaboration of the eudesmane framework to agarofurans and biogenetic-type rearrangement to eremophilanes is outlined.

Item Type: Journal Article
Additional Information: Copyright for this article belongs to Elsevier Science.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 08 Jul 2004
Last Modified: 19 Sep 2010 04:13
URI: http://eprints.iisc.ernet.in/id/eprint/995

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