Enzymatic resolution of dioxygenated dicyclopentadienes: Enantiopure hydrindanes, hydroisoquinolones, diquinanes and application to a synthesis of (+)-coronafacic acid
Data(s) |
29/01/1999
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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 |