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Abstract:

The title compound was prepared in 4 steps from 3β-methoxy-21- hydroxy-5α-pregnan-20-one (1). The required intermediate (4) was obtained using lithium enolate derived from t-butyl acetate. Interesting enough, p-tosyl chloride in pyridine quantitatively converted compound 1 into the a-chloro ketone derivative (2). © 1993, Taylor & Francis Group, LLC. All rights reserved.

Registro:

Documento: Artículo
Título:A facile synthesis of 4-(3β -methoxy-5α -androstan-17β -yl)- 3-pyrrolin-2-one
Autor:Revelli, G.A.; Gros, E.G.
Filiación:Departamento de Quimica Organica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. 2, 1428, Buenos Aires, Argentina
Palabras clave:4 (3beta methoxy 5alpha androstan 17beta yl) 3 pyrrolin 2 one; androstane derivative; unclassified drug; article; drug synthesis; nuclear magnetic resonance
Año:1993
Volumen:23
Número:8
Página de inicio:1111
Página de fin:1119
DOI: http://dx.doi.org/10.1080/00397919308018588
Título revista:Synthetic Communications
Título revista abreviado:Synth. Commun.
ISSN:00397911
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00397911_v23_n8_p1111_Revelli

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Citas:

---------- APA ----------
Revelli, G.A. & Gros, E.G. (1993) . A facile synthesis of 4-(3β -methoxy-5α -androstan-17β -yl)- 3-pyrrolin-2-one. Synthetic Communications, 23(8), 1111-1119.
http://dx.doi.org/10.1080/00397919308018588
---------- CHICAGO ----------
Revelli, G.A., Gros, E.G. "A facile synthesis of 4-(3β -methoxy-5α -androstan-17β -yl)- 3-pyrrolin-2-one" . Synthetic Communications 23, no. 8 (1993) : 1111-1119.
http://dx.doi.org/10.1080/00397919308018588
---------- MLA ----------
Revelli, G.A., Gros, E.G. "A facile synthesis of 4-(3β -methoxy-5α -androstan-17β -yl)- 3-pyrrolin-2-one" . Synthetic Communications, vol. 23, no. 8, 1993, pp. 1111-1119.
http://dx.doi.org/10.1080/00397919308018588
---------- VANCOUVER ----------
Revelli, G.A., Gros, E.G. A facile synthesis of 4-(3β -methoxy-5α -androstan-17β -yl)- 3-pyrrolin-2-one. Synth. Commun. 1993;23(8):1111-1119.
http://dx.doi.org/10.1080/00397919308018588