Reactions of 1-aminocyclopentenes with acyl aryldiazenes give 1:1 enaminic adducts or 1,3,4-oxadiazines. Isolation of these products was not always possible in the reactions of 1-(piperidin-1-yl)- and 1-(pyrrolidin-1-yl)-cyclopentene. Acidic hydrolysis gave 2-(N-acyl-N'-aryl)hydrazinocyclopentanones or 2-arylaminocyclopentenones, depending upon the amine moiety and the cyclic or open chain nature of the adducts.
Reactivity of Cyclopentanone Enamines towards Acyl Aryldiazenes / Benedetti, Fabio; Forchiassin, Mirella; Russo, Claudio; Risaliti, Amerigo. - In: GAZZETTA CHIMICA ITALIANA. - ISSN 0016-5603. - STAMPA. - 115:(1985), pp. 663-668.
Reactivity of Cyclopentanone Enamines towards Acyl Aryldiazenes
BENEDETTI, FABIO;FORCHIASSIN, MIRELLA;RUSSO, CLAUDIO;RISALITI, AMERIGO
1985-01-01
Abstract
Reactions of 1-aminocyclopentenes with acyl aryldiazenes give 1:1 enaminic adducts or 1,3,4-oxadiazines. Isolation of these products was not always possible in the reactions of 1-(piperidin-1-yl)- and 1-(pyrrolidin-1-yl)-cyclopentene. Acidic hydrolysis gave 2-(N-acyl-N'-aryl)hydrazinocyclopentanones or 2-arylaminocyclopentenones, depending upon the amine moiety and the cyclic or open chain nature of the adducts.Pubblicazioni consigliate
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