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Steroids, LII. Configurational Analysis of 16‐Methyl‐19‐nortestosterone Derivatives by Eszter Meskó; György Dombi; Ferenc Lukács; Gyula Schneider is a Chemistry article available to read on EtoBox.

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## Abstract The four possible stereoisomers of 3‐methoxy‐16‐methyloestra‐1,3,5(10)‐trien‐17‐ol (1, 2, 3, 4) were converted into the corresponding 16‐methyl‐19‐nortestosterone analogs (5, 6, 7, 8), which were characterized by their ^1^H‐ and ^13^C‐NMR spectra. The coupling constants __J__~16,17~ and the characteristic ^13^C signals (C‐12, C‐17, C‐18, 16‐CH~3~) clearly confirmed the configurations at C‐16 and C‐17.

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Author

Eszter Meskó; György Dombi; Ferenc Lukács; Gyula Schneider

Publisher

John Wiley and Sons; Wiley (John Wiley & Sons); VCH Verlagsgesellschaft; Wiley (ISSN 0947-3440)

Published

1993

Language

EN

Field

Chemistry (Physical Sciences)