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The absolute configuration of the dicipiene diterpenes
Authors:K.D. Croft  E.L. Ghisalberti  P.R. Jeferries  A.D. Stuart
Affiliation:Department of Organic Chemistry, University of W.A., Nedlands, Western Australia, 6009
Abstract:The absolute configuration of the decipiene diterpenes has been determined by degradation to 4R-4-(2-methoxy-4-methylphenyl)-pentanoic acid. Photolysis of 1,18-diacetoxy-13-oxodecipi-14-ene proceeds through a novel photochemical reaction, formally a [2 + 2] cycloreversion, to generate a key intermediate for the degradation.
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