CIHIDECAR   12529
CENTRO DE INVESTIGACIONES EN HIDRATOS DE CARBONO
Unidad Ejecutora - UE
artículos
Título:
Cyclization of 1,2:3,4-di-O-isopropylidene-?Ñ-D-galacto-1,6-hexodialdo-1,5-pyranose acylhydrazone and semicarbazone
Autor/es:
MIRIAM A. MARTINS ALHO; RICARDO BAGGIO; NORMA B. D'ACCORSO
Revista:
ARKIVOC - ONLINE JOURNAL OF ORGANIC CHEMISTRY
Editorial:
ARKAT USA INC
Referencias:
Lugar: Florida; Año: 2012
ISSN:
1551-7004
Resumen:
The synthesis of 3-N-acyl-1,3,4-oxadiazolines is a well-known reaction and there is a lot of information on this field, however in recent years the number of publications has increased due to the great potential of this heterocyclic ring as chemotherapeutic agent.1,2 Nevertheless, some aspects of heterocyclization reaction are not well known. Looking for new potential biological agents, we studied the differences between heterocyclization of acylhydrazone and semicarbazone obtained from protected carbohydrate derivatives. Also, a hypothesis for their different behavior is proposed.