Stereochemical and carbon-13 NMR investigations. Part 31. Polar and steric long-range transmission effects in cholestanes, cholestenes, and 9-substituted decalins. Carbon-13 nuclear magnetic resonance shifts and force field and linear electric field calculations
- 1 October 1982
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 47 (22), 4216-4221
- https://doi.org/10.1021/jo00143a008
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Synthesis and carbon-13 nuclear magnetic resonance studies of .DELTA.5 saturated 4,4-disubstituted 3-ketosteroidsThe Journal of Organic Chemistry, 1981
- 13C and 1H nuclear magnetic resonance spectroscopy of C-19 and 6β-methyl substituted steroids: long-range shift effects in conformational analysisCanadian Journal of Chemistry, 1979
- Structure-activity relationships for glucocorticoids—IV. Effects of substituents on the overall shape of steroids which bind to the glucocorticoid receptorThe Journal of Steroid Biochemistry and Molecular Biology, 1978
- Analysis of carbon-13 nuclear magnetic resonance for monohydroxy steroids incorporating geometric distortionsThe Journal of Organic Chemistry, 1978