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Abstract:

A short and efficient preparation of 17a-methyl-, 17a-ethyl-, 17a-allyl-, and 17a-benzyl-3β-acetoxy-17a-aza-d-homoandrost-5-en-17-one, as well as 17a-methyl-, 17a-ethyl-, and 17a-allyl-3β-methoxy-17a-aza-s-homoandrost-5-en-17-one from the corresponding androsten-17-one derivatives is described. (Steroids 58:181-184, 1993). © 1993.

Registro:

Documento: Artículo
Título:Synthesis of 17a-alkyl- and 17a-aryl-3β-acetoxy- and 3β-methoxy-17a-aza-d-homoandrost-5-en-17-one
Autor:Revelli, G.A.; Gros, E.G.
Filiación:Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Buenos Aires, Argentina
Palabras clave:17a-aza-d-homoandrost-5-en-17-one derivatives; 13C nuclear magnetic resonance spectra; 1H nuclear magnetic resonance spectra; azasteroids; synthesis; 17a allyl 3beta acetoxy 17a aza d homoandrost 5 en 17 one; 17a allyl 3beta methoxy 17a aza d homoandrost 5 en 17 one; 17a benzyl 3beta acetoxy 17a aza d homoandrost 5 en 17 one; 17a ethyl 3beta acetoxy 17a aza d homoandrost 5 en 17 one; 17a ethyl 3beta methoxy 17a aza d homoandrost 5 en 17 one; 17a methyl 3beta acetoxy 17a aza d homoandrost 5 en 17 one; 17a methyl 3beta methoxy 17a aza d homoandrost 5 en 17 one; 3beta acetoxy 17a aza d homoandrost 5 en 17 one; 3beta methoxy 17a aza d homoandrost 5 en 17 one; azasteroid; unclassified drug; article; carbon nuclear magnetic resonance; drug structure; drug synthesis; mass spectrometry; proton nuclear magnetic resonance; Androstenols; Azasteroids; Magnetic Resonance Spectroscopy; Molecular Structure; Support, Non-U.S. Gov't
Año:1993
Volumen:58
Número:4
Página de inicio:181
Página de fin:184
DOI: http://dx.doi.org/10.1016/0039-128X(93)90066-V
Título revista:Steroids
Título revista abreviado:Steroids
ISSN:0039128X
CODEN:STEDA
CAS:3-methoxy-17-aza-homoandrost-5-ene-17-one, 84300-23-2; Androstenols; Azasteroids
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0039128X_v58_n4_p181_Revelli

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Citas:

---------- APA ----------
Revelli, G.A. & Gros, E.G. (1993) . Synthesis of 17a-alkyl- and 17a-aryl-3β-acetoxy- and 3β-methoxy-17a-aza-d-homoandrost-5-en-17-one. Steroids, 58(4), 181-184.
http://dx.doi.org/10.1016/0039-128X(93)90066-V
---------- CHICAGO ----------
Revelli, G.A., Gros, E.G. "Synthesis of 17a-alkyl- and 17a-aryl-3β-acetoxy- and 3β-methoxy-17a-aza-d-homoandrost-5-en-17-one" . Steroids 58, no. 4 (1993) : 181-184.
http://dx.doi.org/10.1016/0039-128X(93)90066-V
---------- MLA ----------
Revelli, G.A., Gros, E.G. "Synthesis of 17a-alkyl- and 17a-aryl-3β-acetoxy- and 3β-methoxy-17a-aza-d-homoandrost-5-en-17-one" . Steroids, vol. 58, no. 4, 1993, pp. 181-184.
http://dx.doi.org/10.1016/0039-128X(93)90066-V
---------- VANCOUVER ----------
Revelli, G.A., Gros, E.G. Synthesis of 17a-alkyl- and 17a-aryl-3β-acetoxy- and 3β-methoxy-17a-aza-d-homoandrost-5-en-17-one. Steroids. 1993;58(4):181-184.
http://dx.doi.org/10.1016/0039-128X(93)90066-V