论文信息 - Autooxidation of Δ17(20)-20-hydroxy derivatives of steroids. Synthesis of 3β-acetoxy-17α-hydroperoxy-16α-methylpregn-5-en-20-one and its reduction to 17α-hydroxy derivative - 字舞流文

Autooxidation of Δ17(20)-20-hydroxy derivatives of steroids. Synthesis of 3β-acetoxy-17α-hydroperoxy-16α-methylpregn-5-en-20-one and its reduction to 17α-hydroxy derivative

I. Beletskaya | T. Savinova | N. V. Lukashev | L. D. Huy

[1] R. Mayer. Hauptmann, S., Graefe, J.; Remane, H.: Lehrbuch der organischen Chemie. 2. Aufl. 797S., 122 Abb., 58 Tab., 16,7×24 cm. Leipzig: VEB Deutscher Verlag für Grundstoffindustrie 1980. Kunstleder, 52,50 M , 1983 .

[2] R. Wiechert,et al. Reaktionen an 18-Methyl-steroiden , 1971 .

[3] P. R. Enslin. Steroidal analogues of unnatural configuration—II , 1971 .

[4] G. A. Russell,et al. The Oxidation of Carbanions. I. Oxidation of Triaryl Carbanions and Other Tertiary Carbanions1 , 1966 .

[5] H. Viehe,et al. Dichlormethan als Lösungsmittel für Grignard-Reagenzien , 1962 .

[6] J. Iriarte,et al. Steroids. CLXIV.1 Preparation of 6α,16α-Dimethylprogestational and Cortical Hormone Analogs , 1961 .

[7] C. Djerassi,et al. Steroids. CLVI.1 Ring D Unsaturated 16-Methylated Corticosteroids , 1961 .

[8] W. J. Gensler. Lehrbuch der organischen chemie , 1954 .