Correlations between the Stereochemistry and the Chemical Ionization Spectra of Epimeric 3,4-Dimethyl-1,2-cyclopentanediols

C. C. Van De Sande; F. Van Gaever; R. Hanselaer; M. Vandewalle

doi:10.1515/znb-1977-0719

Open Access Published by De Gruyter June 2, 2014

Correlations between the Stereochemistry and the Chemical Ionization Spectra of Epimeric 3,4-Dimethyl-1,2-cyclopentanediols

C. C. Van De Sande , F. Van Gaever , R. Hanselaer and M. Vandewalle

From the journal Zeitschrift für Naturforschung B

https://doi.org/10.1515/znb-1977-0719

The eight epimeric 3,4-dimethyl-l,2-cyclopentanediols have been investigated as bistrimethylsilyl (TMS) ethers and as diacetates by means of isobutane chemical ionization (CI). Correlations between stereochemistry and CI spectra appear to be limited in the case of the TMS ethers. All eight diacetates, however, can be unequivocally identified from their isobutane CI spectra.

Received: 1977-3-28

Published Online: 2014-6-2

Published in Print: 1977-7-1

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Correlations between the Stereochemistry and the Chemical Ionization Spectra of Epimeric 3,4-Dimethyl-1,2-cyclopentanediols

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