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Enantiospecific synthesis of (+)-trans-alpha-himachalene via an intramolecular type II carbonyl ene reaction

Srikrishna, A and Kumar, Ravi P (2008) Enantiospecific synthesis of (+)-trans-alpha-himachalene via an intramolecular type II carbonyl ene reaction. In: Indian Journal of Chemistry Section B, 47 (9). pp. 1414-1422.

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Abstract

Enantiospecific synthesis of (+)-trans-alpha-himachalene starting from (R)-carvone is described. An intramolecular type II carbonyl ene reaction has been employed as the key step for the construction of the bicyclo[5.4.0]undecane ring system.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to National Institute of Science Communication and Information Resources.
Keywords: Enantiospecific synthesis;himachalenes;sesquiterpenes;(R)-carvone;intramolecular ene-reaction.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 18 Nov 2008 10:09
Last Modified: 18 Nov 2008 10:09
URI: http://eprints.iisc.ernet.in/id/eprint/16444

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