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Rotational isomerism in 3-mono-oxygenated and 3,7-di-oxygenated derivatives of N-acetyl-17-aza-D-homoandrost-5-ene

✍ Scribed by Philip J. Dawson; Trevor A. Crabb; Roger O. Williams


Publisher
John Wiley and Sons
Year
1977
Tongue
English
Weight
359 KB
Volume
10
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

The ^1^H n.m.r. spectra of 3‐mono‐oxygenated and 3,7‐dioxygenated N‐acetyl‐17‐aza‐D‐homoandrost‐5‐enes show unequal populations of the amide rotational isomers in chloroform‐d~1~ solution. The populations are dependent upon the orientation of the C‐7 oxygen substituent but are independent of concentration. In pyridine‐d~5~ solution the two rotameric states for each compound are almost equally populated.