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RCM-based approach to (±)-cuparene
A. Srikrishna, , K.R. Prasad
Published in
2007
Volume: 37
   
Issue: 9
Pages: 1511 - 1516
Abstract
An efficient approach to the aromatic sesquiterpene cuparene has been described starting from the readily available β-ionone and employing a combination of epoxide rearrangement-based ring-contraction and ring-closing metathesis reactions as key steps. Copyright © Taylor & Francis Group, LLC.
About the journal
JournalSynthetic Communications
ISSN00397911