Crousse, Benoit, 19..-...., chercheur en chimie médicinale
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Benoit Crousse
Crousse, Benoît
Crousse, Benoit 1967-
VIAF ID: 196270100 ( Personal )
Permalink: http://viaf.org/viaf/196270100
Preferred Forms
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100 0 _
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Benoit Crousse
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100 1 _
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CROUSSE, BENOIT.
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100 1 _
‡a
Crousse, Benoit
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100 1 _
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Crousse, Benoit
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1967-
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100 1 _
‡a
Crousse, Benoit,
‡d
19..-....,
‡c
chercheur en chimie médicinale
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100 1 _ ‡a Crousse, Benoît
4xx's: Alternate Name Forms (3)
Works
| Title | Sources |
|---|---|
| Access to novel amino trifluoromethyl cyclopropane carboxylic acid derivatives |
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| Access to novel functionalized trifluoromethyl β-lactams by ring expansion of aziridines |
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| Alcools fluorés : un milieu parfait pour la fonctionnalisation directe d'aromatiques. |
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| Analogues of key precursors of aspartyl protease inhibitors: synthesis of trifluoromethyl amino epoxides. |
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| applications des réactions radicalaires pour la synthèse des composés carbonylés et des β-acides aminés. |
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| Applications of fluoro-alcohols as reaction media for the synthesis of heterocyclic compounds and perspectives in the design of hybrid materials |
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| Benefits of a Dual Chemical and Physical Activation: Direct aza-Michael Addition of Anilines Promoted by Solvent Effect under High Pressure |
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| Bisulfate Salt-Catalyzed Friedel-Crafts Benzylation of Arenes with Benzylic Alcohols |
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| Carbonylhydrazide-based molecular tongs inhibit wild-type and mutated HIV-1 protease dimerization |
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| Desenvolvimento de Derivados Quinolínicos com Potencial Atividade contra Doenças Infecciosas |
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| Design, synthesis and biological test of fluorine non covalent protéasome inhibitors. |
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| Designed Glycopeptidomimetics Disrupt Protein-Protein Interactions Mediating Amyloid β-Peptide Aggregation and Restore Neuroblastoma Cell Viability. |
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| Development of Quinoline Derivatives with Potential Activity against Infectious Diseases. |
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| Développement de nouveaux dérivés quinoliniques dirigés contre les maladies infectieuses.. |
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| Electrophilic amination of fluoroalkyl groups on azodicarboxylate derivatives. |
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| Facile ring opening of oxiranes with aromatic amines in fluoro alcohols |
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| First synthesis of 10 alpha-(trifluoromethyl)deoxoartemisinin |
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| Fluorinated Alcohols: A New Medium for Selective and Clean Reaction |
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| Fluoro artemisinins: difluoromethylene ketones. |
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| Fluorous 4-N,N-dimethylaminopyridine (DMAP) salts as simple recyclable acylation catalysts. |
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| The fluorous effect in biomolecular applications |
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| Fluorous tagging of DABCO through halogen bonding: recyclable catalyst for the Morita-Baylis-Hillman reaction |
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| From planar chiral o-chloro and o-iodo benzaldehyde tricarbonyl chromium complexes to enantiopure fused hydroisoquinolines and hydroquinolines |
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| In vitro antileishmanial activity of fluoro-artemisinin derivatives against Leishmania donovani. |
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| Influence of the structure of polyfluorinated alcohols on Brønsted acidity/hydrogen-bond donor ability and consequences on the promoter effect |
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| Intramolecular Pd-catalyzed carbocyclization, Heck reactions, and aryl-radical cyclizations with planar chiral arene tricarbonyl chromium complexes. |
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| Des isonitriles aux pyruvamides : nouveaux développements des réactions de Ugi et Phospha-brook |
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| N-Difluoromethyl-triazole as a constrained scaffold in peptidomimetics |
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| N-fluoroalkyls and CF3-cyclopropanes; new peptidomimétics units. |
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| Non Lewis acid catalysed epoxide ring opening with amino acid esters. |
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| Nonmetal catalyzed insertion reactions of diazocarbonyls to acid derivatives in fluorinated alcohols |
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| Nouvelle approche stereoselective aux polyenes conjugues et composes polyinsatures |
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| Novel [1,2]- and [2,3]-Wittig rearrangements of alpha-benzyloxy beta-CF(3)-beta-lactam enolates |
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| A one-pot synthesis of 3-trifluoromethyl-2-isoxazolines from trifluoromethyl aldoxime. |
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| Orally active antimalarials: hydrolytically stable derivatives of 10-trifluoromethyl anhydrodihydroartemisinin. |
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| Preparation of 10-trifluoromethyl artemether and artesunate. Influence of hexafluoropropan-2-ol on substitution reaction. |
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| Réactivité des pentafluorosulfanylalcènes en conditions superacides et synthèse énantiosélective catalysée au rhodium de cyclopropanes fonctionnalisés. |
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| Reactivity of carbon dioxide in hydrofluoroethers: a facile access to cyclic carbonates |
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| Réduction de difluorocyclopropènes par transfert d'hydrogène. Synthèse de difluorocyclopropanes optiquement enrichis |
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| Regioselective Halogenation of Arenes and Heterocycles in Hexafluoroisopropanol. |
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| S(N)/S(N)' competition: selective access to new 10-fluoro artemisinins. |
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| Solubility switch of gold nanoparticles through hydrogen bond association. |
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| Solvent-promoted and -controlled aza-Michael reaction with aromatic amines. |
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| Stereoselective Barbier-type allylation reaction of trifluoromethyl aldimines. |
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| Structure-activity relationships of sugar-based peptidomimetics as modulators of amyloid β-peptide early oligomerization and fibrillization. |
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| Study of the transformation of aminocyclopropanes synthesized with the aim of obtaining 14-azasteroid structures. |
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| Synthèse de nouveaux composés trifluoromethylés azotés. |
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| Synthèse d'hétérocycles fluorées |
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| Synthèse d'inhibiteurs fluorés de carbapénémases : combattre la résistance aux antibiotiques des bactéries à Gram négatif |
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| Synthèse et activité antitumorale d'analogues fluorés de produits naturels issus de Goniothalamus : Nouveaux aspects de synthèse dans les alcools fluorés |
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| Synthèse et réactivité des aziridines trifluorométhylées et des β-lactames contenant un groupement phosphonate. |
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| Synthesis of 2-CF(3)-tetrahydroquinoline and quinoline derivatives from CF(3)-N-aryl-aldimine |
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| Synthesis of novel enantiopure trifluoromethyl nitrogen-containing scaffolds |
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| Synthesis of substituted 8-aminoquinolines and phenanthrolines through a Povarov approach |
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| Triazolamères fluorés : conception, synthèse, études conformationnelles et modulation de l'agrégation de peptides amyloïdes |
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| Trifluoromethyl nitrones: from fluoral to optically active hydroxylamines. |
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| Trifluoromethylated hemiaminals derived from (L)-tartaric acid : synthesis and reactivity. |
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| The use of 4,4,4-trifluorothreonine to stabilize extended peptide structures and mimic β-strands. |
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| α- and β-hydrazino acid-based pseudopeptides inhibit the chymotrypsin-like activity of the eukaryotic 20S proteasome. |
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