François Roblot
Centre national de la recherche scientifique
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Featured researches published by François Roblot.
Phytochemistry | 1993
François Roblot; Thierry Laugel; Michel Lebœuf; André Cavé; Olivier Laprévote
Abstract Chromatography of a hexane extract of Annona muricata seeds led to the isolation of two new γ-lactone acetogenins, epomuricenins A and B, which are the first examples of annonaceous acetogenins having an epoxide and a double bond in the aliphatic chain in place of the usual tetrahydrofuran moiety. The role of this type of acetogenin in the biogenesis of monotetrahydrofuran acetogenins is discussed.
Natural Product Letters | 1997
Hichem Ben Jannet; Zine Mighri; Laurent Serani; Olivier Laprévote; Jean-Christophe Jullian; François Roblot
Abstract Three novel compounds were isolated from the leaves of Ajuga iva (Labiatae). Their structures were established, on the basis of spectroscopic data, as symmetric and asymmetric 1,3-diacyl derivatives of glycerol with 3-hydroxy-tetradecanoic and 3-hydroxy-hexadecanoic acids.
Tetrahedron Letters | 1999
Emerson F. Queiroz; Edna Lucia Meneses Da Silva; François Roblot; Reynald Hocquemiller; Bruno Figadère
Preparations of 1,2-, 1,3-, 1,5-formaldehyde acetals from the corresponding polyhydroxylated annonaceous acetogenins were performed in good yield. Addition of Et3N to a mixture of DMSO and TMSCl is crucial to avoid in situ hydrolysis of the intramolecular acetals.
Rapid Communications in Mass Spectrometry | 1998
Edna Lucia Meneses Da Silva; François Roblot; Reynald Hocquemiller; Laurent Serani; Olivier Laprévote
Collision-induced dissociation (CID) of lithiated molecules generated by liquid SIMS (LSIMS) from two new natural compounds, annoheptocin A and B, led to their structural elucidation. Mass spectrometry (MS) and tandem mass spectrometry (MS/MS) investigations of their acetonide derivatives displayed obvious differences of reactivity of the lithiated dioxane and dioxolane rings towards CID. The 1,3-dioxane (six-membered) ring could be the target of hydrogen rearrangement processes, leading to the formation of a tetrahydrofuran ring through the loss of a molecule of acetone. Copyright
Journal of Essential Oil Research | 1997
Gilbert Founder; Abbas Hadjiakhoondi; François Roblot; Michel Leboeuf; André Cavé; Brigitte Charles
Abstract The essential oils extracted from five Artabotrys species, Annonaceae (A. insignis, A.pierreanus, A. rufus, A. thomsoni and A. venustus) have been examined by GC and GC/MS. The main components of each oil have been identified. Among them, two compounds seem to have a chemotaxonomic significance: cyperenone and 1,5-epoxysalvial-4(l 4)-ene.
Rapid Communications in Mass Spectrometry | 1992
Olivier Laprévote; Christian Girard; Bhupesh C. Das; Thierry Laugel; François Roblot; Michel Leboeuf; André Cavé
Journal of Natural Products | 1983
François Roblot; Reynald Hocquemiller; A. Cavé; Cinthia Simes Moretti
Journal of Natural Products | 1995
Anne Wahl; François Roblot; André Cavé
ChemInform | 2010
E. L. Meneses Da Silva; François Roblot; André Cavé
ChemInform | 2010
Vu Thi Tam Vu Thi Tam; Phan Quan Chi Hieu Phan Quan Chi Hieu; B. Chappe; François Roblot; Bruno Figadère; André Cavé