Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Edward Aig"'
Publikováno v:
Chemischer Informationsdienst. 11
The preparation of a wide variety of 6-substituted trimethoprim analogues was readily accomplished by the reaction of 2,4-diamino-6-substituted-pyrimidines with 2,6-dimethoxy-4-[(N,N-dimethylamino)methyl]phenol at 120--160 degrees C. The less reactiv
Publikováno v:
Chemischer Informationsdienst. 14
Publikováno v:
Journal of medicinal chemistry. 23(5)
The preparation of a wide variety of 6-substituted trimethoprim analogues was readily accomplished by the reaction of 2,4-diamino-6-substituted-pyrimidines with 2,6-dimethoxy-4-[(N,N-dimethylamino)methyl]phenol at 120--160 degrees C. The less reactiv
Publikováno v:
Journal of medicinal chemistry. 26(5)
A new route to 2,4-diamino-5-(4-hydroxybenzyl)pyrimidines has been developed that involves the condensation of 2,4-diamino-5-(hydroxymethyl)pyrimidine with phenols in acidic medium. The use of phenol and its 2,6-dialkyl derivatives produces 5-(4-hydr
Autor:
Edward Aig, Barbara Roth
Publikováno v:
Journal of medicinal chemistry. 30(11)
3,4,5-Triethylacetophenone was synthesized in 60% yield by a Friedel-Crafts reaction from 4-ethylacetophenone and converted to 2,4-diamino-5-(3,4,5-triethylbenzyl)pyrimidine (2), a trimethoprim (1) isostere, by standard techniques. This compound is m
Autor:
Robert Ferone, Justina Z. Strelitz, Barbara Roth, Edward Aig, S. R. M. Bushby, Carl W. Sigel, Arthur P. Phillips, Barbara S. Rauckman
Publikováno v:
Journal of medicinal chemistry. 24(8)
Forty trimethoprim analogues in which the para substituent in the benzene ring was varied were prepared for antibacterial evaluation. All were very potent inhibitors of Escherichia coli dihydrofolate reductase. The similarity of their inhibitory acti
Autor:
Barbara S. Rauckman, Edward Aig, Arthur P. Phillips, R. Ferone, Carl W. Sigel, Justina Z. Strelitz, Barbara Roth, S. R. M. Bushby
Publikováno v:
Chemischer Informationsdienst. 13