Organocatalysed synthesis of isoxazolines initiated by a chemoselective oxa-Michael reaction of N-BocNHOH von Noël, R, Gembus, V, Levacher, V, Brière, J-F

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Organocatalyzed Synthesis of Isoxazolidin-5-ones: The Meldrum's Acid Approach von Postikova, Svetlana, Tite, Tony, Levacher, Vincent, Brière, Jean-François

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Organocatalysed synthesis of isoxazolines initiated by a chemoselective oxa-Michael reaction of N-BocNHOHElectronic supplementary information (ESI) available: Further experimental... von Noël, R, Gembus, V, Levacher, V, Brière, J.-F

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New development of Meyers’ methodology: stereoselective preparation of an axially chiral 5,7-fused bicyclic lactam related to circumdatins/benzomalvins and asperlicins von Penhoat, Maël, Bohn, Pierre, Dupas, Georges, Papamicaël, Cyril, Marsais, Francis, Levacher, Vincent

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ChemInform Abstract: Organocatalyzed Synthesis of Isoxazolines Initiated by a Chemoselective Oxa-Michael Reaction of N-BocNHOH von Noel, R., Gembus, V., Levacher, V., Briere, J.-F.

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Chiral ditopic receptors. Application to palladium-catalyzed allylic alkylation von Bourguignon, Jean, Bremberg, Ulf, Dupas, Georges, Hallman, Kristina, Hagberg, Lars, Hortala, Laurent, Levacher, Vincent, Lutsenko, Serghey, Macedo, Emmanuel, Moberg, Christina, Quéguiner, Guy, Rahm, Fredrik

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Diastereoselective Protonation of Lactam Enolates Derived from (R)-Phenylglycinol. A Novel Asymmetric Route to 4-Phenyl-1,2,3,4-tetrahydroisoquinolines von Philippe, Nicolas, Levacher, Vincent, Dupas, Georges, Quéguiner, Guy, Bourguignon, Jean

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Broadening in the scope of NADH models by using chiral and non chiral pyrrolo [2,3-bl pyridine derivatives von Levacher, V., Benoit, R., Duflos, J., Dupas, G., Bourguignon, J., Queguiner, G.

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Acyl transfer of 8-acetoxy-2-oxazolinylquinoline assisted by hydrogen bonding formation von Hortala, Laurent, Moberg, Christina, Levacher, Vincent, Bourguignon, Jean, Dupas, Georges

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The tert-butyl sulfoximine group as an effective ortho-director of lithiation: ortho-metallated S-( tert-butyl)-S-phenylsulfoximines von Levacher, V., Eriksen, B.Langer, Begtrup, M., Dupas, G., Quéguiner, G., Duflos, J., Bourguignon, J.

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New Efficient Conditions for the Reduction with NADH Models von Vasse, J. L., Charpentier, P., Levacher, V., Dupas, G., Quéguiner, G., Bourguignon, J.

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One Pot Synthesis of Pyrrolo[2,3-b]pyridine Derivatives von Levacher, V., Leroy, C., Dupas, G., Bourguignon, J., Quéguiner, G.

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Study of the Reduction of Enamides with an NADH Model von Leroy, Corine, Levacher, Vincent, Dupas, Georges, Bourguignon, Jean, Quéguiner, Guy

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Synthesis of annealed NADH models in benzothieno[2,3-b]pyridine and pyrido[2,3-b]indole series von LEVACHER, V, BOUSSAD, N, DUPAS, G, BOURGUIGNON, J, QUEGUINER, G

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Broadening in the scope of NADH models by using chiral and non chiral pyrrolo [2,3-b] pyridine derivatives von LEVACHER, V, BENOIT, R, DUFLOS, J, DUPAS, G, BOURGUIGNON, J, QUEGUINER, G

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ChemInform Abstract: Homochiral NADH Models in the Pyrrolo[2,3-b]pyridine Series Bearing One or Two Chiral Auxiliaries. Asymmetric Reduction of Methyl Benzoylformate and N-Acetyl-e... von LEROY, C., LEVACHER, V., DUPAS, G., QUEGUINER, G., BOURGUIGNON, J.

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ChemInform Abstract: Reduction with Non-Chiral and Chiral Biomimetic NADH Models in the Pyrido[2,3-b]indole Series: New Chiral NADH Models Carrying Rigidified Cyclized Structures a... von LEVACHER, V., DUPAS, G., QUEGUINER, G., BOURGUIGNON, J.

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1,2,4-TRIAZINE DERIVATIVES FOR THE TREATMENT OF VIRAL INFECTIONS 124 von JUBAULT, PHILIPPE P, MC GOWAN, DAVID, GRAIG DG, GEMBUS, VINCENT V, LEVACHER, VINCENT V, BONFANTI, JEAN-FRANOIS J-F, HOARAU, CHRISTOPHE C, GUILLEMONT, JRME, EMILE, GEORGES JEG

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ChemInform Abstract: The tert-Butyl Sulfoximine Group as an Effective ortho-Director of Lithiation: ortho-Metalated S-(tert-Butyl)-S-phenylsulfoximines von Levacher, V., Langer Eriksen, B., Begtrup, M., Dupas, G., Queguiner, G., Duflos, J., Bourguignon, J.

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ChemInform Abstract: An Efficient Synthesis of 3-Cyanoquinoline Derivatives von CHARPENTIER, P., LOBREGAT, V., LEVACHER, V., DUPAS, G., QUEGUINER, G., BOURGUIGNON, J.

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