ChemInform Abstract: VERBINDUNG MIT UROTROPIN‐STRUKTUR 50. MITT. CYCLISIERUNGSRK. AUSGEHEND VON CIS‐3,5‐DIAMINO‐CYCLOHEXANOL

Stetter, Hermann; Steffens, Gerd Josef

doi:10.1002/chin.197226211

Chemischer Informationsdienst

1972

DOI: 10.1002/chin.197226211

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ChemInform Abstract: VERBINDUNG MIT UROTROPIN‐STRUKTUR 50. MITT. CYCLISIERUNGSRK. AUSGEHEND VON CIS‐3,5‐DIAMINO‐CYCLOHEXANOL

Hermann Stetter¹,

Gerd Josef Steffens²

Abstract: Durch katalytische Hydrierung des Dinitrophenols (I) wird das an feuchter Luft sehr oxidationsempfindliche Diamin (IIa) gebildet, das zweckmäßig sofort zum stabilen Diacetylderivat (IIb) (82% Ausbeute) acetyliert wird.

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ChemInform Abstract: VERBINDUNG MIT UROTROPIN‐STRUKTUR 50. MITT. CYCLISIERUNGSRK. AUSGEHEND VON CIS‐3,5‐DIAMINO‐CYCLOHEXANOL

Abstract: Durch katalytische Hydrierung des Dinitrophenols (I) wird das an feuchter Luft sehr oxidationsempfindliche Diamin (IIa) gebildet, das zweckmäßig sofort zum stabilen Diacetylderivat (IIb) (82% Ausbeute) acetyliert wird.

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References 1 publication

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