Helvetica Chimica Acta p. 2212 - 2223 (1982)
Update date:2022-08-11
Topics:
Naef, Ferdinand
Decorzant, Rene
Thommen, Walter
A stereocontrolled route to racemic eremophilane and valencane sesquiterpenes is described via a common inetrmediate 15, accessible from an intramolecular Diels-Alder rection. 13C-NMR-shift assignments of the bicyclic intermediates and products are presented.
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