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An enantiospecific total synthesis of (-)-patchouli alcohol
A. Srikrishna,
Published in
2005
Volume: 16
   
Issue: 24
Pages: 3992 - 3997
Abstract
An enantiospecific total synthesis of patchouli alcohol, starting from the readily available monoterpene (R)-carvone, has been accomplished. A tandem double Michael reaction-alkylation sequence and single electron mediated 6-endo trig cyclisation reaction have been employed as key steps. © 2005 Elsevier Ltd. All rights reserved.
About the journal
JournalTetrahedron Asymmetry
ISSN09574166