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.Pubblicazioni consigliate
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