Preparation and carbon‐13 NMR study of 3‐ and 20‐methylene analogues of steroid hormones
20‐Methylpregna‐4,20‐dien‐3‐one and the corresponding 17α‐hydroxy, 20‐hydroxymethyl and 17α‐hydroxy‐20‐hydroxymethyl derivatives were prepared from the 20‐keto compounds by Wittig reaction or a modified Simmons‐Smith reaction. The 13C NMR spectra of these steroids and of 3‐methylene derivatives are...
Guardado en:
Autores principales: | Gonzalez, M.D., Burton, G. |
---|---|
Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_07491581_v26_n11_p963_Gonzalez |
Aporte de: |
Ejemplares similares
-
Preparation and carbon‐13 NMR study of 3‐ and 20‐methylene analogues of steroid hormones
por: González, Mario Daniel, et al.
Publicado: (1988) -
Preparation and NMR characterization of new substituted benzo[a]phenazines
por: Benedetti-Doctorovich, V., et al. -
Carbon-13 nuclear magnetic resonance spectral data of steroidal vicinal ketols and related compounds
Publicado: (1991) -
Carbon-13 nuclear magnetic resonance spectral data of steroidal vicinal ketols and related compounds
por: Doller, D., et al. -
Synthesis and NMR Studies of Some Steroidal Isoxazoles
por: Giacopello, Sergio, et al.
Publicado: (1992)