Abstract
The sesquiterpenoic alcohol nerolidol was separated into its 4 stereoisomers by MPLC of the diastereomeric (1 5,4R)-camphanoates. An analytical GC method was found by which both the enantiomeric pairs of (Z)- and (E)-nerolidol are resolved on a chiral cyclodextrin stationary phase. The olfactoric properties of the nerolidol stereoisomers were investigated. © 1992, Walter de Gruyter. All rights reserved.
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APA
Schubert, V., Dietrich, A., Ulrich, T., & Mosandl, A. (1992). The Stereoisomers of Nerolidol: Separation, Analysis and Olfactoric Properties. Zeitschrift Fur Naturforschung - Section C Journal of Biosciences, 47(3–4), 304–307. https://doi.org/10.1515/znc-1992-3-422
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