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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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Official URL: http://dx.doi.org/10.1016/S0040-4039(98)02465-4

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
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.ernet.in/id/eprint/38587

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