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


Autoria(s): Mehta, Goverdhan; Reddy, Srinivasa D
Data(s)

29/01/1999

Resumo

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.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/38587/1/Enzymatic_Resolution_of_Dioxygenated.pdf

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.

Publicador

Elsevier Science

Relação

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

http://eprints.iisc.ernet.in/38587/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed