Articles

THE PREPARATION OF α-FARNESENE HYDROPEROXIDES FOR THE STUDY OF SUPERFICIAL SCALD

Article number
464_24
Pages
177 – 182
Language
Abstract
The short and efficient synthesis of four alpha-farnesene autoxidation products is described.
Geraniol was converted to the conjugated trienyl hydroperoxide (3) via the known trienol (2). Trienyl hydroperoxide (3) was efficiently cyclised in the presence of oxygen and an intiator to afford the very labile endoperoxy hydroperoxide (5), a route which mimics alpha-farnesene autoxidation.
Reduction of (5) gave the endoperoxy alcohol (4).


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Publication
Authors
S. Fielder, M. S. Sherburn, Daryl D. Rowan
Keywords
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