Issue 0, 1966

Hydroxy-steroids. Part VIII. The conformations and infrared spectra of 3,5-diols and 3,5,6-triols

Abstract

The nature and extent of the intramolecular hydrogen bonding in some 3,5-diols, 3,5,6-triols, and related esters obtained from steroids of unnatural configuration are readily discerned by examining the O–H stretching bands of dilute solutions under high dispersion. From the results the hydroxyl groups' configurations and the preferred conformations of these compounds can be deduced.

Article information

Article type
Paper

J. Chem. Soc. C, 1966, 1864-1866

Hydroxy-steroids. Part VIII. The conformations and infrared spectra of 3,5-diols and 3,5,6-triols

G. M. L. Cragg, G. D. Meakins and W. Zaharia, J. Chem. Soc. C, 1966, 1864 DOI: 10.1039/J39660001864

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements