Reaction of enaminodimidones with x-cyanocinnamonitriles and their ester analogues
Bulletin of Faculty of Pharmacy-Cairo University. 1991; 29 (3): 9-13
em Inglês
| IMEMR
| ID: emr-95323
ABSTRACT
The reaction of several N-Substituted enaminodimidones with alpha, B-unsaturated nitriles is described. N-Aryl-enaminodimidones were found to react differently from their N-alkyl analogues giving the quinoline B-enaminotriles [3 a-m] and their esters with the former and the arylideneamine [4 a,b] in case of the latters. Likewise, the reaction products were found to be depending on polarity and temperature. 1[H] nmr, ir and microanalysis were consistent with the chemical structure of the products
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Nitrilas
Idioma:
Inglês
Revista:
Bull. Fac. Pharm.-Cairo Univ.
Ano de publicação:
1991
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