The reactivity of alfa-beta-unsaturated p-Tosylhydrazones toward ion cyanide as nucleophile. In a aqueous-dichloromethane two-phases reaction, using benzyltriethyammonium chloride as a phase-transfer catalyst, we obtained hydrocyanation of tosylhydrazones of cycloexanone and other unconjugated substrates, while the C=N of conjugated one, resists nucleophilic attack of cyanide ion.

Attempted Nucleophilic Attack of Cyanide Ion on alfa-beta-unsaturated p-Tosylhydrazones / Bellesia, Franco; Pagnoni, Ugo Maria; A., Pinetti. - In: GAZZETTA CHIMICA ITALIANA. - ISSN 0016-5603. - STAMPA. - 111:(1981), pp. 431-434.

Attempted Nucleophilic Attack of Cyanide Ion on alfa-beta-unsaturated p-Tosylhydrazones.

BELLESIA, Franco;PAGNONI, Ugo Maria;
1981

Abstract

The reactivity of alfa-beta-unsaturated p-Tosylhydrazones toward ion cyanide as nucleophile. In a aqueous-dichloromethane two-phases reaction, using benzyltriethyammonium chloride as a phase-transfer catalyst, we obtained hydrocyanation of tosylhydrazones of cycloexanone and other unconjugated substrates, while the C=N of conjugated one, resists nucleophilic attack of cyanide ion.
1981
111
431
434
Attempted Nucleophilic Attack of Cyanide Ion on alfa-beta-unsaturated p-Tosylhydrazones / Bellesia, Franco; Pagnoni, Ugo Maria; A., Pinetti. - In: GAZZETTA CHIMICA ITALIANA. - ISSN 0016-5603. - STAMPA. - 111:(1981), pp. 431-434.
Bellesia, Franco; Pagnoni, Ugo Maria; A., Pinetti
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/646046
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