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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 12, 1982 - Issue 7
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Original Articles

Synthesis of Methyl Dihydrojasmonate. Ester Directed Baeyer-Villiger Oxidation

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Pages 501-505 | Published online: 05 Dec 2006
 

Abstract

The distinguished organoleptic properties of the jasmonoids have helped foment development of synthetic routes.1 In one of our recent approaches to methyl dihydrojasmonate (1) we assimulated and integrated the acid-catalyzed rearrangement process2 of cyclopentadiene-acrylic acid adducts into our scheme.

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