Zobrazeno 1 - 10
of 27
pro vyhledávání: '"C. Landras"'
Publikováno v:
Tetrahedron. 52:10427-10440
Whereas thermal cyclisation of variously substituted 2,3-diarylacrylazides easily provided a new way to 3-aryl-isoquinolones, nitration of these compounds mainly led to corresponding 3-aryl-4-nitro-isoquinolones. After reduction into 4-amino-3-aryl-i
Autor:
Alain Pierré, C. Landras, Ghanem Atassi, Laurence Kraus-Berthier, Yves Rolland, R. Jasztold‐Howorko, Stéphane Léonce, Claude Guillonneau, Emile Bisagni, Nicolas Guilbaud
Publikováno v:
Chemical and Pharmaceutical Bulletin. 44:2169-2172
Starting from 2-(6-methoxy-1-methylcarbazol-2-yl)ethylamine and diethyl-2, 6-pyridine dicarboxylate, the title compounds were obtained through five or six steps. The new compounds retained significant cytotoxicity towards various tumor cell lines, bu
Publikováno v:
ChemInform. 24
2,6-Diaminotoluene (3a) and 2,6-diamino-p-xylene (3c) led to 2-methyl (and 2,5-dimethyl)-3-acetylamino-phenylhydrazines 5a,b. Fischer indolization of their hydrazones 6a,b and 7a,b derived from 4-methoxycy-clohexanone and 4-piperidone, and subsequent
Autor:
Nicolas Guilbaud, Prost Jf, Laurence Kraus-Berthier, Stéphane Léonce, Alain Pierre, Ghanem Atassi, R. Jasztold‐Howorko, Yves Rolland, C. Landras, Emile Bisagni
Publikováno v:
ChemInform. 25
Starting from 2-(2-aminoethyl)-6-methoxy-1-methylcarbazole, ethyl 9-methoxy-5-methyl-6H-pyrido[4,3-b]carbazole-1-carboxylate was obtained through a three-step sequence. This compound and its 6-methyl derivative react with (dialkylamino)alkylamines to
Publikováno v:
ChemInform. 27
Whereas thermal cyclisation of variously substituted 2,3-diarylacrylazides easily provided a new way to 3-aryl-isoquinolones, nitration of these compounds mainly led to corresponding 3-aryl-4-nitro-isoquinolones. After reduction into 4-amino-3-aryl-i
Autor:
Claude Guillonneau, Laurence Kraus-Berthier, R. Jasztold‐Howorko, Emile Bisagni, C. Landras, Alain Pierré, Ghanem Atassi, Yves Rolland, Stéphane Léonce, Nicolas Guilbaud
Publikováno v:
ChemInform. 28
Starting from 2-(6-methoxy-1-methylcarbazol-2-yl)ethylamine and diethyl-2, 6-pyridine dicarboxylate, the title compounds were obtained through five or six steps. The new compounds retained significant cytotoxicity towards various tumor cell lines, bu
Publikováno v:
Journal of Heterocyclic Chemistry. 29:1573-1576
2,6-Diaminotoluene (3a) and 2,6-diamino-p-xylene (3c) led to 2-methyl (and 2,5-dimethyl)-3-acetylamino-phenylhydrazines 5a,b. Fischer indolization of their hydrazones 6a,b and 7a,b derived from 4-methoxycy-clohexanone and 4-piperidone, and subsequent
Autor:
R. Jasztold‐Howorko, Prost Jf, Yves Rolland, Emile Bisagni, Stéphane Léonce, Alain Pierre, C. Landras, Laurence Kraus-Berthier, Ghanem Atassi, Nicolas Guilbaud
Publikováno v:
Journal of medicinal chemistry. 37(15)
Starting from 2-(2-aminoethyl)-6-methoxy-1-methylcarbazole, ethyl 9-methoxy-5-methyl-6H-pyrido[4,3-b]carbazole-1-carboxylate was obtained through a three-step sequence. This compound and its 6-methyl derivative react with (dialkylamino)alkylamines to
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Akademický článek
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