Issue 12, 1977

Proton magnetic resonance studies of sterols. Assignment of methyl signals of C27, C28, C29 analogues

Abstract

The 1H n.m.r. chemical shifts, obtained at 100 MHz, of a number of cholestane, ergostane, and stigmastane analogues have been assigned. Deviations from additivity of substituent effects upon the angular methyl chemical shifts were noted for certain 14,15 disubstituted compounds. Resolution of signals from the C-25 methyl groups of stigmastanes, but not of the ergostanes, was observed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1977, 1403-1406

Proton magnetic resonance studies of sterols. Assignment of methyl signals of C27, C28, C29 analogues

T. A. Wittstruck, J. K. Sliwowski and E. Caspi, J. Chem. Soc., Perkin Trans. 1, 1977, 1403 DOI: 10.1039/P19770001403

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