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

Mehta, Goverdhan ; Srinivasa Reddy, D. (1999) Enzymatic resolution of dioxygenated dicyclopentadienes: enantiopure hydrindanes, hydroisoquinolones, diquinanes and application to a synthesis of (+)-coronafacic acid Tetrahedron Letters, 40 (5). pp. 991-994. ISSN 0040-4039

Full text not available from this repository.

Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

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

Abstract

A 5,10-dioxygenated-tricyclo[5.2.1.02,6]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.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Enzymes; Enantiomeric Purity; Indanes; Hydrindanes
ID Code:28953
Deposited On:18 Dec 2010 05:46
Last Modified:18 Dec 2010 05:46

Repository Staff Only: item control page