0000000000851763

AUTHOR

François-xavier Felpin

0000-0002-8851-246x

showing 3 related works from this author

Recyclable heterogeneous palladium catalysts in pure water: sustainable developments in Suzuki, Heck, Sonogashira and Tsuji-Trost reactions

2010

This review summarizes the progress made essentially these last ten years on heterogeneous palladium catalysis in pure water. The work covers four important palladium-catalyzed transformations for carbon-carbon bond formation: Suzuki, Heck, Sonogashira and Tsuji-Trost reactions. The discussion focuses on the efficiency and reusability of the heterogeneous catalysts as well as on the experimental conditions from a sustainable chemistry point of view. The review is introduced by a discussion on mechanistic aspects inherent to heterogeneous catalysis.

Green chemistryheterogeneous palladium catalysts010405 organic chemistrywaterSonogashira couplingchemistry.chemical_elementGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryHeterogeneous catalysis01 natural sciences7. Clean energySuzuki reaction -Tsuji-Trost reaction0104 chemical sciencesCatalysisTsuji–Trost reaction[ CHIM.CATA ] Chemical Sciences/CatalysisHeck reactionchemistrySuzuki reactionHeck reactionOrganic chemistrySonogashira reactionComputingMilieux_MISCELLANEOUSPalladium
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ChemInform Abstract: Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji-Tros…

2010

This review summarizes the progress made essentially these last ten years on heterogeneous palladium catalysis in pure water. The work covers four important palladium-catalyzed transformations for carbon-carbon bond formation: Suzuki, Heck, Sonogashira and Tsuji-Trost reactions. The discussion focuses on the efficiency and reusability of the heterogeneous catalysts as well as on the experimental conditions from a sustainable chemistry point of view. The review is introduced by a discussion on mechanistic aspects inherent to heterogeneous catalysis.

Green chemistryChemistrySonogashira couplingOrganic chemistrychemistry.chemical_elementGeneral MedicineBond formationHeterogeneous catalysisPalladiumReusabilityCatalysisChemInform
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1,1prime-Binaphthyl-2-methylpyridinium-based peroxophosphotungstate salts: synthesis, characterization, and their use as oxidation catalysts

2009

A series of 1,1′-binaphthyl-2-methylammonium and pyridinium salts 6, 7, and 8 was synthesized through the coupling reaction of 2-(bromomethyl)-1,1′-binaphthalene (5) with the dendritic tetraallyl pyridinedicarbinol dendron 2 as well as triethylamine and 4-tert-butylpyridine. Tetraallyl pyridinedicarbinol dendron 2 was prepared by allylation of commercially available diethyl pyridine-3,5-dicarboxylate (1). The allylation of 2 with allyltrimethylsilane in the presence of boron trifluoride was unsuccessful, as tetraallyl pyridinedicarbinol trifluoroboron adduct 3 was obtained instead of expected hexaallylpyridine compound 4. The catalytic hydrogenation of allyl groups of the ammonium salt of 2…

oxidationCyclohexanolSalt (chemistry)010402 general chemistry01 natural sciencesCoupling reactionCatalysisdendrimersInorganic Chemistrychemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysis[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistrypolyoxometalatesTriethylamineBoron trifluorideComputingMilieux_MISCELLANEOUSchemistry.chemical_classification[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryThioanisole[CHIM.CATA]Chemical Sciences/Catalysishomogeneous catalysis0104 chemical scienceschemistryPyridinium
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