Reactions of uridine and 4-thiouridine derivatives with some-halo esters
Egyptian Journal of Pharmaceutical Sciences. 1996; 37 (1-6): 291-302
em Inglês
| IMEMR
| ID: emr-40799
ABSTRACT
Uridine and 4-thiouridine were converted into the corresponding 2,3-o-isopropylidene-5-thiocyanato derivatives. Then, each resulted derivative was reacted individually with both of ethyl alpha- chloroacetoacetate, ethyl alpha-bromobenzoylacetate and ethyl bromo pyruvate. Furthermore, these 5-thiocyanato products were transformed into the corresponding 5-mercapto analogues. The produced analogues were undergo ring formation to give the corresponding 4,5-cyclized pyrimidine derivatives
Buscar no Google
Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Tiouridina
/
Uridina
/
Ésteres
Idioma:
Inglês
Revista:
Egypt. J. Pharm. Sci.
Ano de publicação:
1996
Similares
MEDLINE
...
LILACS
LIS