Cleavage reactions of 4-thiazolidinone-2-thiones: reactions with 5-arylhydrazono-4thiazolidinone-2-thiones
Egyptian Journal of Chemistry. 1985; 28 (6): 497-503
en Inglés
| IMEMR
| ID: emr-5654
ABSTRACT
In continuation to our interest in the chemistry of thiazolidinone ring systems, owing to their considerable biological activities, we re-Port here on the behaviour of 5-arylhydrazono-4-thiazolodinone-2-thiones [6] la and b toward the action of a variety of nucleophilic reagents. Thus, subjecting la and b to the action of aliphetic amines affected elimination of the arylhydrazono group with concomitant ring cleavage to afford the thiooxalic acid amides 2a-c. This is in analogy with arylhydrazono group elimination in 4-arylhydrazono5-imino-3-pyrazolinones by amines
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Tiazoles
Idioma:
Inglés
Revista:
Egypt. J. Chem.
Año:
1985
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