Zobrazeno 1 - 10
of 219
pro vyhledávání: '"C. Luu Duc"'
Publikováno v:
ChemInform. 26
Several series of benzimidazole and imidazole derivatives have been synthesized and their biological activity evaluated. Their ability to inhibit human placental aromatase activity was tested in vitro. Ten of the tested compounds are more active towa
Autor:
J, Chantegrel, J C, Albuquerque, V L, Guarda, M, Perrissin, M C A, Lima, S L, Galdino, S S, Brandão, F, Thomasson, I R, Pitta, C, Luu-Duc
Publikováno v:
Annales pharmaceutiques francaises. 60(6)
Synthesis and physico-chemical properties of some 3-benzyl- and 3-phenacyl-4-thioxo-5-benzylidenethiazolidin-2-one derivatives are described. Fifteen new compounds were synthesized from thiazolidin-2-one by thionation of the 4-carbonyle, alkylation o
Autor:
S S, Brandão, V L, Guarda, I R, Pitta, J, Chantegrel, M, Perrissin, V M, Souza, S L, Galdino, F, Thomasson, M C, Lima, L F, Leite, C, Luu-Duc
Publikováno v:
Bollettino chimico farmaceutico. 139(2)
Synthesis and physico-chemical properties of six 5-arylidène-3-benzyl-1-methyl-2-thioxoimidazolidin-4-ones and three 2-arylidene-6-nitro-2H-1,4-benzothiazin-3(4H)-ones have been described. These new compounds were synthetised by Knoevenagel condensa
Autor:
S S, Brandão, J A, Rocha Filho, J, Chantegrel, J F, Albuquerque, E A, Ximenes, S L, Galdino, I R, Pitta, M, Perrissin, C, Luu-Duc
Publikováno v:
Annales pharmaceutiques francaises. 55(5)
Synthesis and physico-chemical properties of four 3-benzyl or 3-(4-chlorobenzyl)-4-thioxo-5-arylazo-imidazolidin-2-ones, five 3-(4-nitrobenzyl)-5-arylidenethiazolidine-2,4-diones and three 3-(4-phenyl-phenacyl)-4-thioxo-5-arylidenethiazolidin-2-ones
Autor:
Suely Lins Galdino, Vera Lúcia de Miranda Guarda, M. Perrissin, C. Luu Duc, Ivan da Rocha Pitta
Publikováno v:
Heterocyclic Communications. 3
Publikováno v:
Annales pharmaceutiques francaises. 55(5)
The synthesis and physico-chemical properties of fourteen 4-thio-5-arylidene-thiazolidine-2-ones and eight 3-(4-bromophenacyl)-4-thio-5-arylidene-thiazolidine-2-ones are described. These products were synthetized by the aldolisation-crotonisation rea
Autor:
J F, Albuquerque, A, Albuquerque, C C, Azevedo, F, Thomasson, L S, Galdino, J, Chantegrel, M T, Catanho, I R, Pitta, C, Luu-Duc
Publikováno v:
Die Pharmazie. 50(6)
Synthesis and physico-chemical properties of six 3-(4-bromophenacyl)-5-arylidene-thiazolidine-2,4-diones and eight 3-(4-chlorobenzyl)-5-arylidene-4-thio-imidazolidine-2-ones are described. These products were synthesized by an aldolisation-crotonisat
Autor:
D L, Barros Costa, J, Chantegrel, M C, Alves de Lima, J M, Cavalcanti Albuquerque, R M, Correa Lima, S L, Galdino, I R, Pitta, C, Luu-Duc
Publikováno v:
Journal de pharmacie de Belgique. 50(1)
Synthesis and physico-chemical properties of nine 3-(4-fluoro or chlorobenzyl)-5-arylidène-imidazolidine-2,4-diones, four 3-(4-fluoro or bromobenzyl)-5-arylidène-thiazolidine-2,4-diones and three 3-)4-bromophénacyl)-5-arylidène-thiazolidine-2,4-
Publikováno v:
Annales pharmaceutiques francaises. 53(5)
The synthesis and the physico-chemical properties of four 3-(4-bromophenacyl)-5-arylidene-thiazolidine-2,4-diones, two 3-(4-bromobenzyl)-5-arylidene-thiazolidine-2,4-diones and seven 3-(4-chlorobenzyl)-5-arylidene-4-thio-imidazolidine-2-ones were des
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 49(7-8)
Several series of benzimidazole and imidazole derivatives have been synthesized and their biological activity evaluated. Their ability to inhibit human placental aromatase activity was tested in vitro. Ten of the tested compounds are more active towa