Please use this identifier to cite or link to this item:
Title: Enantiospecific synthesis of (+)-trans-⍺-himachalene via an intramolecular type II carbonyl ene reaction
Authors: Srikrishna, A
Kumar, P Ravi
Keywords: Enantiospecific synthesis;Himachalenes;Sesquiterpenes;(R)-carvone;Intramolecular ene-reaction
Issue Date: Sep-2008
Publisher: CSIR
Abstract: Enantiospecific synthesis of (+)-trans-⍺-himachalene starting from (R)-carvone is described. An intramolecular type II carbonyl ene reaction has been employed as the key step for the construction of the bicyclo[5.4.0]undecane ring system.
Page(s): 1414-1422
ISSN: 0376-4699
Appears in Collections:IJC-B Vol.47B(09) [September 2008]

Files in This Item:
File Description SizeFormat 
IJCB 47(9) 1414-1422.pdf134.46 kBAdobe PDFView/Open

Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.