Jacqueline Gleye
University of Toulouse
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Featured researches published by Jacqueline Gleye.
Phytochemistry | 1983
Claude Moulis; Komar R. Wirasutisna; Jacqueline Gleye; Philippe Loiseau; E. Stanislas; Christian Moretti
Abstract From Almeidea guyanensis , besides N -methylatanine, N -methylflindersine, N -methylkhaplofoline and 4-demethyl- N -methylatanine, a new 2-quinolone, almeine, has been isolated and its structure elucidated as 4-isopropenyl- N -methyl-3,4-dihydrofuro-2-quinolone.
Phytochemistry | 1995
Marie-Thérèse Fauvel; Anne Bousquet-Mélou; Claude Moulis; Jacqueline Gleye; Søren Rosendal Jensen
Abstract A new iridoid glucoside, namely 2′-caffeoyl mussaenosidic acid has been isolated from leaves of Avicennia germinans along with the known compounds 2′-cinnamoyl mussaenosidic acid and verbascoside. The structure of the new compound was established by spectroscopic methods.
Phytochemistry | 1981
M.Th. Fauvel; Jacqueline Gleye; Claude Moulis; F. Blasco; E. Stanislas
Abstract The following substances were isolated from the leaves of Melicope indica : N -methylatanine dictamnine, evolitrine, meliternatin, melibentin and a new flavonoid which was shown to be 3,5,8-trimethoxy-6,7: 3′,4′-dimethylenedioxyflavone by its spectroscopic properties.
Phytochemistry | 1990
Joël Boustie; Claude Moulis; Jacqueline Gleye; Isabelle Fouraste; Philippe Servin; Maryse Bon
Abstract The structure and absolute configuration of fraxinellonone isolated from Fagaropsis glabra was established as 3α-(3′-furanyl)-3α,7-dimethyl-4,5-dihydro-1,6-isobenzofurandione, by NMR and CD comparison with fraxinellone. Complete carbon assignments for fraxinellone and isofraxinellone were achieved by 13 C- 1 H COSY experiments.
Phytochemistry | 1977
Claude Moulis; Jacqueline Gleye; E. Stanislas
Abstract Besides the known magnoflorine, four new protoberberines were isolated from leaves of Isopyrum thalictroides . Their structures were deduced from spectral data. The names pseudoberberine, pseudocoptisine, pseudocolumbamine and dehydropseudocheilanthifoline are proposed for them.
Phytochemistry | 1990
Amri Bakhtiar; Jacqueline Gleye; Claude Moulis; Isabelle Fouraste; E. Stanislas
Abstract From the stem bark of Galipea trifoliata were identified swertisin, isoswertisin, 2″-O-xylosylisoswertisin, vicenin-2, schaftoside, isoschaftoside and two new compounds: 6,8 di-C-glucosylgenkwanin and 2‴-O-xylosyl-6,8-di-C-glucosylgenkwanin.
Phytochemistry | 1987
K.R. Wirasutisna; Jacqueline Gleye; Claude Moulis; E. Stanislas; C. Moretti
Abstract In addition to phebalosin and ramosin, the air-dried stem and root barks of Galipea trifoliata contain a third previously unreported coumarin identified as 7-isopentenyloxy-8-( trans -1′,2′-epoxy-3′-methyl-3′-butenyl)coumarin.
Phytochemistry | 1983
E. Gomes; G. Dellamonica; Jacqueline Gleye; Cl. Moulis; Jean Chopin; E. Stanislas
Abstract From the leaves of Vepris heterophlylla, trans-sinapic acid methyl ester, 2″-O-glucosylisovitexin, 2″-O-glucosylvitexin, isovitexin
Phytochemistry | 1995
Joël Boustie; Marie-José Respaud; Claude Moulis; Catherine Lavaud; Jacqueline Gleye; Isabelle Fouraste
Abstract Phytochemical studies of the alcoholic-soluble portion of Fagaropsis glabra have resulted in the isolation of fagaropsine, a degraded limonoid glycoside. Its absolute structure was elucidated as 1-O-β- d -glucopyranosyl-4α-(3′-furanyl)-7β-hydroxy-4aα,8α-dimethyl-4,4a,5,6,7,8-hexahydro-3-benzopyran-2-one on the basis of spectral data.
Phytochemistry | 1994
Amri Bakhtiar; Jacqueline Gleye; Claude Moulis; Isabelle Fouraste
Abstract From the stem bark of Galipea trifoliata the glycoflavones 2″- O -xylosylswertisin, 2″- O -glucosylswertisin, 2″- O -glucosylisoswertisin and 2″- O -β- d -xylosyl-8- C -β- d -galactosylapigenin were identified.