Jean Favre-Bonvin
University of Lyon
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Featured researches published by Jean Favre-Bonvin.
Phytochemistry | 1971
Victor Plouvier; Jean Favre-Bonvin
Resume 80 composes rencontres a letat naturel ont ete classes suivant leur structure: monoterpenes methylcyclopentanoides, iridoides proprement dits, seco-iridoides. Pour chacun deux sont indiquees la repartition chez les vegetaux, la structure et la stereochimie (si elle est elucidee). Un tableau taxinomique groupe les familles et genres de plantes a iridoides. Les proprietes generales de ces composes, leur recherche chez les vegetaux et leur action biologique sont brievement decrites. Les experiences effectuees sur leur biosynthese sont mentionnees: de lacide mevalonique aux iridoides et seco-iridoides, de la loganine aux seco-iridoides et aux alcaloides indoliques.
Phytochemistry | 1981
Marie-Louise Bouillant; Jean-Louis Pittet; Jacques Bernillon; Jean Favre-Bonvin; Noël Arpin
Abstract The chemical structure of the mycosporin isolated from Ascochyta pisi, Cladosporium herbarum and Septoria nodorum was established as mycosporin-2 glucoside.
Phytochemistry | 1984
Frédéric Jullien; Bernard Voirin; Jacques Bernillon; Jean Favre-Bonvin
Abstract Six highly oxygenated flavones have been isolated from the leaves of Mentha piperita . Five known compounds, 5-hydroxy-6,7,8,4′-tetramethoxyflavone, 5,4′-dihydroxy-6,7,8-trimethoxyflavone, 5,3′-dihydroxy-6,7,8,4′-tetramethoxyflavone, 5-hydroxy-6,7,8,3′,4′-pentamethoxyflavone and 5,3′,4′-trihydroxy-6,7,8-trimethoxyflavone, are reported for the first time in the genus Mentha . The sixth compound has been identified as 5,6-dihydroxy-7,8,3′,4′-tetramethoxyflavone by UV, NMR and mass spectra.
Phytochemistry | 1974
Noël Arpin; Jean Favre-Bonvin; Wolfgang Steglich
Abstract The brown—red colour of the external layer of Fomes, fomentarius is basically due to three compounds. The main constituent, fomentariol, has the structure 7,4′-di(3-hydroxy-1-propenyl)-purpurogallin.
Tetrahedron Letters | 1983
Mourad Kaouadji; Jean Favre-Bonvin
Resume The title compound, a new trimer of coniferyl alcohol, has been isolated from defatted seeds of Herpetospermum caudigerum Wall. (Cucubitaceae). Its structure was elucidated by spectroscopic means as rel -( 7′S , 8′S , 7″S , 8″S -4,9,4′,4″-tetrahydroxy-5,5′,5″-trimethoxy-7-oxo-8.3′,7′.0.9″,8′.8″,9′.0.7″-lignoid.
Phytochemistry | 1986
T.R. Seetharaman; Bernard Voirin; Jean Favre-Bonvin
Abstract The structure of triumboidin isolated from Triumfetta rhomboidea as scutellarein 7- O - l -arabinorhamnoside is inconsistent with the spectral data. Its true structure has been established as scutellarein 6-xyloside 7-rhamnoside. 1 H and 13 C NMR and FAB-MS data for scutellarein 7- O -α- l -rhamnoside have also been provided.
Tetrahedron Letters | 1984
Mourad Kaouadji; Jean Favre-Bonvin
Abstract The title compound, a new pentamer of coniferyl alcohol has been isolated from seeds of Herpetospermum caudigerum Wall. (Cucurbitaceae). Its structure was established by spectroscopic means as 4,9,9′,9″,9″′,4″″-hexahydroxy-5,5′,5″,5″′,5″″-pentamethoxy-7.0.4′,8.3′,7′.0.4″,8′.3″,7″.0.4 8″.3″′,7″′.0.9″″,8″8′.″″--lignoid.
Phytochemistry | 1981
Jacques Fayret; Jacques Bernillon; Marie-Louise Bouillant; Jean Favre-Bonvin; Noël Arpin
Abstract The three reproductive forms of Gnomonia leptostyla synthesize mycosporin-2 ring and open forms. The chemical structures were determined from NMR and MS data.
Phytochemistry | 1984
Bernard Voirin; Jean Favre-Bonvin; V. Indra
Abstract Majoranin isolated from Majorana hortensis and characterized earlier as 5,7,4′-trihydroxy-6,8,3′-trimethoxyflavone was found to be different from sudachitin of the same structure. Its true structure has been established as 5,6,4′-trihydroxy-7,8,3′-trimethoxyflavone (thymonin) by spectral data and direct comparison.
Tetrahedron Letters | 1978
Jean Favre-Bonvin; Mourad Kaouadji; Anne-Marie Mariotte
Resume herpetotriol, a new lignan isolated from Herpetospermum caudigerum , has the structure of a trimer, ( 2 ), of coniferyl alcohol.