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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 16, 1986 - Issue 10
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Original Articles

Efficient Syntheses of β-Sesquiphellandrene and Zingiberenol Employing a Tandem Arylation-Multistep Reduction-Hydrolysis Sequence1

Joseph R. Flisak Department of Chemistry, Olson Laboratories, Rutgers University Newark, New Jersey, 07102
&
Stan S. Hall Department of Chemistry, Olson Laboratories, Rutgers University Newark, New Jersey, 07102
Pages 1217-1228 | Published online: 05 Dec 2006
 
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Abstract

The title sesquiterpenes are synthesized in one step from the common intermediate 4-(6-methyl-5-hepten-2-yl)-2-cyclohexen-1-one, which is prepared using a one-pot tandem arylation-multistep reduction-hydrolysis sequence.

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