Zobrazeno 1 - 10
of 19
pro vyhledávání: '"J. C. Milhavet"'
Autor:
S. Hansel, M. H. Sportouch, M. De Méo, Michèle Laget, Marcel Castegnaro, J C Milhavet, Gérard Duménil
Publikováno v:
International Archives of Occupational and Environmental Health. 69:109-114
Handling genotoxic compounds commonly used in cancer chemotherapy generates contaminated wastes that require decontamination before disposal. Chemical methods are an alternative and/or a complement to incineration for the treatment of wastes and spil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88b0d5f46dbdd16d12a8a215b95180ff
https://doi.org/10.1007/s004200050124
https://doi.org/10.1007/s004200050124
Autor:
Robert Snoeck, Jean-Pierre Chapat, Jean-Claude Teulade, Yves Blache, A. Elhakmaoui, Graciela Andrei, Olivier Chavignon, Erik De Clercq, A. Gueiffier, J. C. Milhavet
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:1937-1940
A series of 3-substituted imidazo[1,2-a]pyridines wa synthesized as potential antiviral agents. Compound 10b and, to a lesser extent, 10c showed activity against both TK+ and TK− strains of varicella-zoster virus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad0db8d847f8ed94f0e03cdc887dcbf1
https://doi.org/10.1016/s0960-894x(01)80538-2
https://doi.org/10.1016/s0960-894x(01)80538-2
Autor:
Gérard Dauphin, A. Gueiffier, H. Viols, Yves Blache, J. P. Chapat, J. C. Milhavet, Olivier Chavignon, J. C. Teulade
Publikováno v:
Journal of Heterocyclic Chemistry. 31:161-166
In this paper, we report the results of heterocyclizations in the pyrido[2,3-b]pyrazine series to give the pyrido[2,3-e] or [3,2-e]pyrrolo[1,2-a]pyrazine. The Clauson-Kaas reaction on 2,3-diaminopyridine is investigated; regioselectivity on the 3-ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2853afec59466393a8edc1e389f6641
https://doi.org/10.1002/jhet.5570310127
https://doi.org/10.1002/jhet.5570310127
Autor:
Olivier Chavignon, J. P. Chapat, H. Viols, Jean C. Teulade, Alain Gueiffier, M. Madesclaire, Yves Blache, Gérard Dauphin, J. C. Milhavet
Publikováno v:
ChemInform. 22
The reaction of nitrosyl chloride with 6- and 8-acetamido-7-methylimidazo[1, 2-a]pyridine (7g-i) reveal clear differences of reactivity of these isomeric structures. After bifunctionalization of the imidazolic moiety, the 6-acetamido derivatives do n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b25241487f69c59e953f9b06124e3c3c
https://doi.org/10.1002/chin.199118179
https://doi.org/10.1002/chin.199118179
Publikováno v:
ChemInform. 25
The pyrrolo[2,1-f][1,6]naphthyridine, pyrrolo[1,2-a][1,8]- and [1,5]naphthyridines along with their corresponding 2,3- and 1,2-dihydrocompounds are synthesized from naphthyridinium dicyanomethylides and dimethyl acetylenedicarboxylate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c66d550f88ebee979fd7d405e3ffae15
https://doi.org/10.1002/chin.199413067
https://doi.org/10.1002/chin.199413067
Autor:
Gérard Dauphin, J. P. Chapat, Olivier Chavignon, Yves Blache, J. C. Milhavet, J. C. Teulade, H. Viols, A. Gueiffier
Publikováno v:
ChemInform. 26
In this paper, we report the results of heterocyclizations in the pyrido[2,3-b]pyrazine series to give the pyrido[2,3-e] or [3,2-e]pyrrolo[1,2-a]pyrazine. The Clauson-Kaas reaction on 2,3-diaminopyridine is investigated; regioselectivity on the 3-ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::074ad03eae65266d72eafa47939a993e
https://doi.org/10.1002/chin.199511188
https://doi.org/10.1002/chin.199511188
Autor:
Jean-Pierre Chapat, J. C. Teulade, Graciela Andrei, A. Elhakmaoui, Yves Blache, J. C. Milhavet, Olivier Chavignon, Robert Snoeck, A. Gueiffier, E. de Clercq
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d724b0253bb57894d084e32f019c3e5
https://doi.org/10.1002/chin.199509205
https://doi.org/10.1002/chin.199509205
Autor:
J. C. Milhavet, Alain Gueiffier, M. Madesclaire, H. Viols, Yves Blache, Olivier Chavignon, Gérard Dauphin, Jean C. Teulade, J. P. Chapat
Publikováno v:
Chemical and Pharmaceutical Bulletin. 38:2352-2356
The reaction of nitrosyl chloride with 6- and 8-acetamido-7-methylimidazo[1, 2-a]pyridine (7g-i) reveal clear differences of reactivity of these isomeric structures. After bifunctionalization of the imidazolic moiety, the 6-acetamido derivatives do n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce6a9e7d0021def29a79bef35393779e
https://doi.org/10.1248/cpb.38.2352
https://doi.org/10.1248/cpb.38.2352
Autor:
J. P. Chapat, A. Elhakmaoui, Yves Blache, Olivier Chavignon, Jean C. Teulade, Gérard Dauphin, J. C. Milhavet, Henry Viols, Alain Gueiffier
Publikováno v:
HETEROCYCLES. 38:283
The synthesis of somes imidazo[1',2':1,2]pyrido[5,6-b]pyrazines by treatment of quaternary salts of pyrido[2,3-b]pyrazines with ammonium acetate in acetic acid media is described
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91f35fff6c9446115520ca024852cb19
https://doi.org/10.3987/com-93-6521
https://doi.org/10.3987/com-93-6521
Publikováno v:
HETEROCYCLES. 36:2513
4-Methylthiopyrrolo[1,2-a][1,8]naphthyridine and pyrrolo[1,2-a]-quinoline were prepared by an intramolecular cyclisation in acidic media of 1-methylsulfinyl-1-methylthio-2-[3-(2-(1-pyrrolyl)pyridin or phenyl)]ethylene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d0b27083dd38e53b305d540ce6237da
https://doi.org/10.3987/com-93-6475
https://doi.org/10.3987/com-93-6475