Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Henri Moskowitz"'
Autor:
Joe¨lle Rayrargue, Henri Moskowitz, Fatima Zaari, Jean-Franç¸ois Berrien, Marie-Noe¨lle Raymond
Publikováno v:
Tetrahedron Letters. 40:3367-3370
Methoxyallylcopper reagents substituted in α and/or β position of methoxy group reacted regiospecifically with MVK to give γ-1, 4 adducts, i.e. ketoenolethers. γ substituted methoxyallylcopper reagents gave mixtures of γ-1, 4 and α-1, 4 adducts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad66f74646fd57afec397fba508ec703
https://doi.org/10.1016/s0040-4039(99)00485-2
https://doi.org/10.1016/s0040-4039(99)00485-2
Autor:
Michel Coquillay, J. L. Avril, Bernard Marcot, Colette De Rango, Henri Moskowitz, Joëlle Mayrargue
Publikováno v:
New Journal of Chemistry. 23:743-748
Hydroxylamine reacts with 2-(2,3-dimethoxyphenyl)-2-propynylcyclohexanone 1 and leads, not to the expected oxime, but to a N-hydroxyaminonitrone 5, according to a reverse-Cope or a 1,3-azaprotiocyclotransfer (APT) mechanism. The deprotection of the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea400340e6ef9a9e46be82d7bf091ac4
https://doi.org/10.1039/a901896d
https://doi.org/10.1039/a901896d
Publikováno v:
ChemInform. 23
Pummerer's ketone 1 is obtained with an overall yield of 55 % by the following sequence: Claisen rearrangement of an arylcyclohexylether 3; allylic oxidation of the methylcycloalkylphenolic derivative 4b, then spontaneous cyclisation during demethyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::520bb259291342b0ff2e92109f40d61e
https://doi.org/10.1002/chin.199243159
https://doi.org/10.1002/chin.199243159
Publikováno v:
ChemInform. 23
effective and straightforward route has been accomplished for the synthesis of hexahydrodibenzofurans based on rearrangement of a spirodihydrocoumarin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dd65c25214319f55f1d98ad43607902
https://doi.org/10.1002/chin.199238141
https://doi.org/10.1002/chin.199238141
Autor:
M.H. Munos, Alain Fournet, Henri Moskowitz, Joëlle Mayrargue, Jean-Charles Gantier, Reynald Hocquemiller
Publikováno v:
ChemInform. 26
Synthesis of an antileishmanial alkaloid and related compounds by using various epoxide-forming reactions is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63a3463f9c72aedbbb5c58948e88a11a
https://doi.org/10.1002/chin.199518262
https://doi.org/10.1002/chin.199518262
Publikováno v:
ChemInform. 29
Lithium diisopropylamide, reacts with trifluoromethylketones either as a base in polar solvents or as a hydride donor in hexane. In the presence of tert -Butyldimethylsilyl chloride, Lithium diisopropylamide allows the transformation of trifluorometh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ec5c8033cb16e2f642739e52ce68e96
https://doi.org/10.1002/chin.199818065
https://doi.org/10.1002/chin.199818065
Publikováno v:
ChemInform. 30
A short synthesis of C4 trifluoro-substituted 1,2,4-trioxanes with antimalarial potential is reported. This is the first example using a trifluorosilylated enol ether function as a protective group for a trifluoromethyl carbonyl.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a641f098a10acca4997a04488e0471b
https://doi.org/10.1002/chin.199907182
https://doi.org/10.1002/chin.199907182
Autor:
Bernard Marcot, Colette De Rango, Henri Moskowitz, J. L. Avril, Michel Coquillay, Joëlle Mayrargue
Publikováno v:
ChemInform. 30
Hydroxylamine reacts with 2-(2,3-dimethoxyphenyl)-2-propynylcyclohexanone 1 and leads, not to the expected oxime, but to a N-hydroxyaminonitrone 5, according to a reverse-Cope or a 1,3-azaprotiocyclotransfer (APT) mechanism. The deprotection of the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3188e7cb6a1e0b16957958d271982839
https://doi.org/10.1002/chin.199941115
https://doi.org/10.1002/chin.199941115
Publikováno v:
ChemInform. 32
The synthesis of 2-substituted-trifluoromethylquinolines from aniline, trifluoromethylanilines, 3-aminoquinoline and trifluoromethylquinaldines is reported. In vitro antileishmanial evaluation of 2-alkyl, 2-alkenyl and 2-epoxypropyl-trifluoromethylqu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9569c1fac9c47bcfe4b2ec0c87abd4ee
https://doi.org/10.1002/chin.200139150
https://doi.org/10.1002/chin.200139150
Publikováno v:
Synthetic Communications. 22:1783-1792
Pummerer's ketone 1 is obtained with an overall yield of 55 % by the following sequence: Claisen rearrangement of an arylcyclohexylether 3; allylic oxidation of the methylcycloalkylphenolic derivative 4b, then spontaneous cyclisation during demethyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92ed936105101f0688cb3ed5a9c4f90d
https://doi.org/10.1080/00397919208020498
https://doi.org/10.1080/00397919208020498