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Téléphone
05 40 00 64 41
Groupe de recherche
Synthèse organique et substances naturelles
Statut
Permanent
Poste
Chercheur
Batiment
A12
Etage
RDC Ouest
Publications
(). Zn(OTf)2-Catalyzed Dehydrocoupling of Terminal Alkynes with Diisopropylaminoborane: A Modular Route to Mono- and Dialkynylboranes. In Advanced Synthesis and Catalysis (Vol. 368, Issue 10, p. e70504). https://doi.org/10.1002/adsc.70504
(). Photoinduced Reduction and Deuteration of Aryl Halides with NHC-Boranes. In European Journal of Organic Chemistry (Vol. 28, Issue 43, p. e202500543). https://doi.org/10.1002/ejoc.202500543
(). Self-Healing and Creep-Resistant Injectable Hydrogel from Aminoborinate Chemistry and Phase Separation. In ACS Materials Letters (Vol. 7, Issue 7, p. 2534-2540). https://doi.org/10.1021/acsmaterialslett.5c00532
(). Photoinduced Deprotection of 2-Nitrophenylneopentyl Glycol Boronates Enables Light-Triggered Polycondensation of Siloxanes. In Chemistry A European Journal (Vol. 31, Issue 6, p. e202404577). https://doi.org/10.1002/chem.202404577
(). Improved conditions for the synthesis of tertiary fluorides using a KF/H2SO4 combination. In Journal of Fluorine Chemistry (Vol. 279, p. 110338). https://doi.org/10.1016/j.jfluchem.2024.110338
(). Post-Functionalization of Organoboranes by Cu-Catalyzed Azide Alkyne [3+2]-Cycloaddition Reaction. In European Journal of Organic Chemistry (Vol. 27, Issue 37, p. e202400580). https://doi.org/10.1002/ejoc.202400580
(). The Cyclic Imine Core Common to the Marine Macrocyclic Toxins Is Sufficient to Dictate Nicotinic Acetylcholine Receptor Antagonism. In Marine Drugs (Vol. 22, Issue 4, p. 149). https://doi.org/10.3390/md22040149
(). Metal-Free Defluoroborylation of 3,3-Difluoropropenes. In European Journal of Organic Chemistry (Vol. 26, Issue 40, p. e202300731). https://doi.org/10.1002/ejoc.202300731
(). Synthesis of Tertiary Fluorides through an Acid-Mediated Deoxyfluorination of Tertiary Alcohols. In Journal of Organic Chemistry (Vol. 88, Issue 20, p. 14527-14539). https://doi.org/10.1021/acs.joc.3c01558
(). Recent Advances in the Synthesis of Borinic Acid Derivatives. In Molecules (Vol. 28, Issue 6, p. 2660). https://doi.org/10.3390/molecules28062660
(). Hydrohalogenation of Unactivated Alkenes Using a Methanesulfonic Acid/Halide Salt Combination. In Synthesis Germany (Vol. 54, Issue 5, p. 1413-1421). https://doi.org/10.1055/s-0040-1719856
(). In situ generation of radical initiators using amine-borane complexes for carbohalogenation of alkenes. In Chemical Communications (Vol. 58, Issue 13, p. 2124-2127). https://doi.org/10.1039/d1cc06390a
(). Hydrofluorination of Alkenes: A Review. In Chemistry an Asian Journal (Vol. 16, Issue 6, p. 563-574). https://doi.org/10.1002/asia.202001403
(). Correction: Amine-borane complex-initiated SF5Cl radical addition on alkenes and alkynes (Beilstein Journal of Organic Chemistry (2021) 17 (1725-1726) DOI: 10.3762/bjoc.16.256). In Beilstein Journal of Organic Chemistry (Vol. 17, p. 1725-1726). https://doi.org/10.3762/bjoc.17.120
(). Amine-borane complex-initiated SF5Cl radical addition on alkenes and alkynes. In Beilstein Journal of Organic Chemistry (Vol. 16, p. 3069-3077). https://doi.org/10.3762/BJOC.16.256
(). Non-biaryl atropisomerism at the C-B bond in sterically hindered aminoarylboranes. In Organic and Biomolecular Chemistry (Vol. 18, Issue 16, p. 3007-3011). https://doi.org/10.1039/d0ob00421a
(). Zirconium-Catalyzed Synthesis of Alkenylaminoboranes: From a Reliable Preparation of Alkenylboronates to a Direct Stereodivergent Access to Alkenyl Bromides. In Organic Letters (Vol. 22, Issue 7, p. 2838-2843). https://doi.org/10.1021/acs.orglett.0c00908
(). Magnesium-Catalyzed Tandem Dehydrogenation-Dehydrocoupling: An Atom Economical Access to Alkynylboranes. In Chemistry A European Journal (Vol. 26, Issue 15, p. 3236-3240). https://doi.org/10.1002/chem.201905772
(). Magnesium promoted autocatalytic dehydrogenation of amine borane complexes: A reliable, non-cryogenic, scalable access to boronic acids. In Tetrahedron (Vol. 75, Issue 2, p. 164-171). https://doi.org/10.1016/j.tet.2018.11.036
(). Recent Advances in [Cp*MIII] (M = Co, Rh, Ir)-Catalyzed Intramolecular Annulation Through C–H Activation. In European Journal of Organic Chemistry (Vol. 2018, Issue 42, p. 5777-5794). https://doi.org/10.1002/ejoc.201800298
(). Rhodium(III)-Catalyzed Synthesis of Spiropiperidine Derivatives via C-H Activation. In Journal of Organic Chemistry (Vol. 83, Issue 4, p. 2324-2340). https://doi.org/10.1021/acs.joc.7b03252
(). Mild rhodium(iii)-catalyzed intramolecular annulation of benzamides with allylic alcohols to access azepinone derivatives. In Chemical Communications (Vol. 54, Issue 46, p. 5891-5894). https://doi.org/10.1039/c8cc03319f
(). Rhodium(III)-Catalyzed Synthesis of Aryl Spirocycles by Aromatic C-H Activation/Intramolecular Heck-Type Reaction. In Advanced Synthesis and Catalysis (Vol. 357, Issue 18, p. 3880-3884). https://doi.org/10.1002/adsc.201500768
(). Hypervalent-Iodine-Mediated Synthesis of 1,2-Dispirodienones: Experimental and Theoretical Investigations. In European Journal of Organic Chemistry (Vol. 2015, Issue 34, p. 7494-7503). https://doi.org/10.1002/ejoc.201501160
(). Enantioselective synthesis of spiroimines by asymmetric decarboxylative alkylation/isomerization/[3+2]-cycloaddition reaction of azidoalkenes. In European Journal of Organic Chemistry (Vol. 2014, Issue 34, p. 7716-7720). https://doi.org/10.1002/ejoc.201403161
(). Synthesis of γ-butenolides and α,β-unsaturated γ-butyrolactams by addition of vinylogous nucleophiles to Michael acceptors. In Tetrahedron (Vol. 70, Issue 16, p. 2595-2615). https://doi.org/10.1016/j.tet.2014.01.057
(). Hypervalent iodine-mediated oxidative cyclisation of p-hydroxy acetanilides to 1,2-dispirodienones. In Chemical Communications (Vol. 49, Issue 98, p. 11542-11544). https://doi.org/10.1039/c3cc47171c
(). Benefit of 13-desmethyl spirolide C treatment in triple transgenic mouse model of Alzheimer disease: Beta-amyloid and neuronal markers improvement. In Current Alzheimer Research (Vol. 10, Issue 3, p. 279-289). https://doi.org/10.2174/1567205011310030007
(). Catalytic enantioselective vinylogous Mukaiyama-Michael addition of 2-silyloxyfurans to cyclic unsaturated oxo esters. In Journal of Organic Chemistry (Vol. 78, Issue 6, p. 2289-2300). https://doi.org/10.1021/jo3020648
(). Studies on the asymmetric Birch reductive alkylation to access spiroimines. In Tetrahedron Letters (Vol. 53, Issue 11, p. 1370-1372). https://doi.org/10.1016/j.tetlet.2012.01.008
(). 6,6-Spiroimine analogs of (-)-gymnodimine A: Synthesis and biological evaluation on nicotinic acetylcholine receptors. In Organic and Biomolecular Chemistry (Vol. 9, Issue 23, p. 8112-8118). https://doi.org/10.1039/c1ob06257c
(). Vinylogous Mukaiyania-Michael Reactions between 2-SiLyIoxyfurans and cyclic enones or unsaturated oxo esters. In European Journal of Organic Chemistry (Issue 28, p. 5471-5481). https://doi.org/10.1002/ejoc.201000504
(). Carboazidation of chiral allylsilanes: Experimental and theoretical investigations. In Chemistry A European Journal (Vol. 14, Issue 9, p. 2744-2756). https://doi.org/10.1002/chem.200701401
(). Total synthesis of hyacinthacine A1 and 3-epi-hyacinthacine A1. In Organic Letters (Vol. 7, Issue 13, p. 2587-2590). https://doi.org/10.1021/ol050713s
(). Radical animation with sulfonyl azides: A powerful method for the formation of C-N bonds. In Chemistry A European Journal (Vol. 10, Issue 15, p. 3606-3614). https://doi.org/10.1002/chem.200400027
(). Allylsilanes in organic synthesis - Recent developments. In European Journal of Organic Chemistry (Issue 15, p. 3173-3199). https://doi.org/10.1002/ejoc.200300789
(). Free-radical functionalisation of vinylcyclopropanes. In Tetrahedron (Vol. 59, Issue 43, p. 8543-8550). https://doi.org/10.1016/j.tet.2003.09.013
(). On the stereochemistry of β-elimination of β-silyl azides. In Tetrahedron Letters (Vol. 44, Issue 37, p. 6995-6998). https://doi.org/10.1016/S0040-4039(03)01800-8
(). Stereoselective intermolecular carboazidation of chiral allylsilanes. In Organic Letters (Vol. 4, Issue 24, p. 4257-4260). https://doi.org/10.1021/ol026824y