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- W2028113324 abstract "Nitrierung von 1-Methyl-Δ1.3.5(10)-ostratrienol-(17β)-acetat (1) fuhrt zu einem Gemisch der 2-Nitro- und 4-Nitro-Verbindung (2, 3); die entsprechenden Amine (4 bzw. 5) lassen sich durch Diazotieren, Verkochen und Verseifen in 1-Methyl-Δ1.3.5(10)-ostratriendiol-(2.17β) (8) und -diol-(4.17β) (9) uberfuhren, deren ostrogene Wirksamkeit untersucht wird. — Versuche, 1-Methyl-4-hydroxy-Δ1.3.5(10)-trien-steroide aus Δ1.4-Dienon-(3)-Verbindungen mit einer Sauerstoff-Funktion an C-4 durch Reduktion und Dienol-Benzol-Umlagerung oder aus Δ2-Enon-(4)-steroiden uber das Oxim durch Semmler-Wolff-Aromatisierung darzustellen, verliefen negativ." @default.
- W2028113324 created "2016-06-24" @default.
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- W2028113324 date "1966-04-07" @default.
- W2028113324 modified "2023-10-05" @default.
- W2028113324 title "1-Methyl-Δ1.3.5(10)-östratriendiol-(4.17β) und 1-Methyl-Δ1.3.5(10)-östratriendiol-(2.17β)" @default.
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- W2028113324 doi "https://doi.org/10.1002/jlac.19666920121" @default.
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