Enantiospecific synthesis of pacifigorgianes

Srikrishna, A and Dethe, Dattatraya H (2012) Enantiospecific synthesis of pacifigorgianes. In: Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry, 51 (2). pp. 345-355.

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Abstract

Enantiospecific synthesis of the sesquiterpenes pacifigorgianes has been described. (R)-Carvone has been employed as the chiral starting material and an entropy assisted ring-closing metathesis reaction by Grubbs first generation catalyst was employed as the key strategy.

Item Type:	Journal Article
Publication:	Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry
Publisher:	National Institute of Science Communication and Information Resources
Additional Information:	Copyright of this article belongs to National Institute of Science Communication and Information Resources.
Keywords:	Pacifigorgianes;bicyclo[4.3.0]nonanes;carvone;entropy effect; ring-closing metathesis;enantiospecific synthesis
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	28 Mar 2012 06:01
Last Modified:	28 Mar 2012 06:01
URI:	http://eprints.iisc.ac.in/id/eprint/44092

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