Enzymatic resolution of dioxygenated dicyclopentadienes: Enantiopure hydrindanes, hydroisoquinolones, diquinanes and application to a synthesis of (+)-coronafacic acid

Mehta, Goverdhan and Reddy, Srinivasa D (1999) Enzymatic resolution of dioxygenated dicyclopentadienes: Enantiopure hydrindanes, hydroisoquinolones, diquinanes and application to a synthesis of (+)-coronafacic acid. In: Tetrahedron Letters, 40 (5). pp. 991-994.

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Abstract

A 5, 10-dioxygenated-tricyclo[5.2.1.0(2,6)]decane derivative 6 has yielded to efficient enzymatic resolution to provide a range of chiral building blocks, whose absolute configuration has been determined through a total synthesis of naturally occuring (+)-coronafacic acid. (C) 1999 Elsevier Science Ltd. All rights reserved.

Item Type:	Journal Article
Publication:	Tetrahedron Letters
Publisher:	Elsevier Science
Additional Information:	Copyright of this article belongs to Elsevier Science.
Keywords:	Enzymes;Enantiomeric purity;Indanes/Hydrindanes
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	23 Jun 2011 06:12
Last Modified:	23 Jun 2011 06:12
URI:	http://eprints.iisc.ac.in/id/eprint/38587

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