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Steroids, XLII. Configurational analysis of 3-methoxy-16-methylestra-1,3,5(10)-trien-17-ol derivatives

✍ Scribed by Meskó, Eszter ;Schneider, Gyula ;Dombi, György ;Zeigan, Dieter

Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
332 KB
Volume
1990
Category
Article
ISSN
0947-3440

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✦ Synopsis

Abstract

The four possible isomers of 16‐hydroxymethyl‐3‐methoxyestra‐1,3,5(10)‐trien‐17‐ol 5a, 6a, 7a, 8a were converted into the corresponding 16‐methyl analogues 4a, 11a, 12a, 13a, which were characterized from their ^1^H‐ and ^13^C‐NMR spectra. The results permit a configurational correlation with 16‐methyl derivatives reported in the literature.

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