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- W2605544785 abstract "Durch Reaktion der Titelverbindung (I) mit Aziridin in Gegenwart von Wasser entsteht durch Ringöffnung überraschenderweise das N-freie Keton (III) (24% Ausbeute), während das erwartete Aziridinid (IIa) sich in Spuren gerade noch nachweisen läßt. Dagegen entsteht mit Diäthylamin als Hauptprodukt das Amid (IIb) (75%) und als Nebenprodukt (IIa) (13%)." @default.
- W2605544785 created "2017-04-28" @default.
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- W2605544785 date "1970-03-17" @default.
- W2605544785 modified "2023-10-16" @default.
- W2605544785 title "ChemInform Abstract: CYCLOPROPENONCHEMIE 4. MITT. RINGOEFFNUNGSRK. VON 2-AETHYL-3-PHENYL-CYCLOPROPENON" @default.
- W2605544785 cites W2152941731 @default.
- W2605544785 doi "https://doi.org/10.1002/chin.197011116" @default.
- W2605544785 hasPublicationYear "1970" @default.
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