Structural information from OH stretching frequencies—IX. The influence of γ-alkyl substituents on the different OH rotamers in saturated axial cyclohexanols
- 1 January 1982
- journal article
- Published by Elsevier in Spectrochimica Acta Part A: Molecular Spectroscopy
- Vol. 38 (7) , 743-749
- https://doi.org/10.1016/0584-8539(82)80061-5
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Structural information from OH stretching frequencies—VIII. On the use of the frequency shift νd(CCl4CS2) of saturated tertiary alcoholsSpectrochimica Acta Part A: Molecular Spectroscopy, 1982
- Structural information from OH stretching frequencies—VII. Preferential OH-rotamers in saturated tertiary alcoholsSpectrochimica Acta Part A: Molecular Spectroscopy, 1981
- Structural information from OH stretching frequencies—VI. On the presence of different rotamers in alkyl substituted tertiary adamantanol-2 and bicylo[3.3.1]nonanol-9 compoundsSpectrochimica Acta Part A: Molecular Spectroscopy, 1981
- Structural information from OH stretching frequencies—V. On the presence of different rotamers in substituted tertiary cyclohexanol compoundsSpectrochimica Acta Part A: Molecular Spectroscopy, 1980
- Structural information from OH stretching frequencies—IV. The fixation effect in saturated tertiary alcoholsSpectrochimica Acta Part A: Molecular Spectroscopy, 1980
- Structural information from OH stretching frequencies—III. The ratio axial/equatorial hydroxyl for cyclohexanol and 1-methyl cyclohexanolSpectrochimica Acta Part A: Molecular Spectroscopy, 1979
- Oxidation of secondary alcohols in diethyl ether with aqueous chromic acid. Convenient procedure for the preparation of ketones in high epimeric purityThe Journal of Organic Chemistry, 1971