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

Meskó Eszter | Zendy; Schneider Gyula | Zendy; Dombi György | Zendy; Zeigan Dieter | Zendy

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

Author(s) -

Meskó Eszter,

Schneider Gyula,

Dombi György,

Zeigan Dieter

Publication year - 1990

Publication title -

liebigs annalen der chemie

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 0170-2041

DOI - 10.1002/jlac.199019900181

Subject(s) - chemistry , hydroxymethyl , stereochemistry , nmr spectra database , computational chemistry , two dimensional nuclear magnetic resonance spectroscopy , spectral line , medicinal chemistry , quantum mechanics , physics

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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