Literatura académica sobre el tema "Réaction à plusieurs composants"
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Artículos de revistas sobre el tema "Réaction à plusieurs composants"
Fougeyrollas, Patrick y Claire Dumont. "Construction identitaire et résilience en réadaptation". Articles 22, n.º 1-2 (1 de diciembre de 2010): 22–26. http://dx.doi.org/10.7202/045023ar.
Texto completoABDELHAFFAR, W., W. NCIBI y R. FAKHFAKH. "VALIDATION TRANSCULTURELLE D'UN QUESTIONNAIRE EVALUANT LE STRESS LIE AU DIABETE EN ARABE DIALECTAL TUNISIEN". EXERCER 34, n.º 192 (1 de abril de 2023): 156–62. http://dx.doi.org/10.56746/exercer.2023.192.156.
Texto completoVaisblat, Noga, Nicholas B. Harris, Korhan Ayranci, Rick Chalaturnyk y Matthew Power. "Rock compositional control on geomechanical properties of the Montney Formation, Western Canadian Basin". Bulletin of Canadian Energy Geoscience 71, n.º 2 (1 de septiembre de 2024): 143–70. http://dx.doi.org/10.35767/gscpgbull.71.2.143.
Texto completoMoser, Klaus. "Les modèles d'effet publicitaire". Recherche et Applications en Marketing (French Edition) 13, n.º 1 (marzo de 1998): 25–34. http://dx.doi.org/10.1177/076737019801300102.
Texto completoVivien, Laurent, Delphine Marris-Morini, Eric Cassan, Carlos Alonso-Ramos, Charles Baudot, Frédéric Bœuf y Bertrand Szelag. "Circuits intégrés photoniques silicium". Photoniques, n.º 93 (septiembre de 2018): 18–22. http://dx.doi.org/10.1051/photon/20189318.
Texto completoKopp, Christophe, Stéphane Bernabe, Mohand Achouche y Sébastien Le Beux. "Photonique sur silicium : des réseaux à fibres au traitement optique de données". Photoniques, n.º 98 (septiembre de 2019): 24–27. http://dx.doi.org/10.1051/photon/20199824.
Texto completoORCEL, V., F. ADELINE-DUFLOT, J. LE BRETON, S. BROSSIER, A. TAHA y V. RENARD. "VACCINATION CONTRE LA COVID-19 ET RISQUE ALLERGIQUE : DES DONNEES POUR LA MEDECINE GENERALE". EXERCER 32, n.º 170 (1 de febrero de 2021): 79–85. http://dx.doi.org/10.56746/exercer.2021.170.79.
Texto completoDieulle, Laurence. "Fiabilité de plusieurs groupes de composants avec maintenance à des instants aléatoires". Comptes Rendus de l'Académie des Sciences - Series I - Mathematics 327, n.º 11 (diciembre de 1998): 943–46. http://dx.doi.org/10.1016/s0764-4442(99)80140-2.
Texto completoDesquesnes, Marc y Laurent Tresse. "Evaluation de la sensibilité de la PCR pour la détection de l'ADN de Trypanosoma vivax selon divers modes de préparation des échantillons sanguins". Revue d’élevage et de médecine vétérinaire des pays tropicaux 49, n.º 4 (1 de abril de 1996): 322–27. http://dx.doi.org/10.19182/remvt.9504.
Texto completoCollin-Lachaud, Isabelle, Maud Herbert y Pauline de Pechpeyrou. "Substitution d’enseignes". Décisions Marketing N° 65, n.º 1 (1 de enero de 2012): 57–69. http://dx.doi.org/10.3917/dm.065.0057.
Texto completoTesis sobre el tema "Réaction à plusieurs composants"
Jia, Shuanglong. "Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives". Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLY012/document.
Texto completoMulticomponent reactions play a significant role in organic chemistry. They allow the reaction occur between three or more starting materials, providing adducts which are considered as elements for the syntheses of complex molecules with bioactive compounds. Benifiting from their diversity, these reactions are considered as valuable tools for the preparation of libraries of organic structures in the pharmaceutical research and total synthesis of natural products field.The Passerini reaction, combined with Michael addition and cyclisation, served an easy access to γ-butyrolactones with good yields. The Passerini adducts of aromatic aldehydes act as nucleophiles in Michael additions with acrylonitrile. The reaction proceeds together with hydrolysis of the ester. The resulting γ-hydroxynitrile can be cyclized under acidic conditions to afford γ- butyrolactones.The NH-aryl hydrazones derived from trifluoroacetaldehyde hemiacetal can be involved in efficient Mannich type reactions with formaldehyde and aromatic aldehydes. The resulting hydrazones are useful building blocks for the preparation of trifluoromethyl substituted 1,2-diazine derivatives under heating with β-ketoesters.Moreover, naphthalene derivatives may be obtained through Tsuji-Trost reaction. This reaction may involve the formation of a palladium p-allyl complex followed by a base promoted β-hydride elimination. This reaction combined with the condensation of fused cyclic ketones with nitromethane and the functionalization of the resulting nitrocycloalkenes (Michael, Mannich...) constitute a very powerful synthetic tool for the formation of 1-substituted naphtalenes
Jia, Shuanglong. "Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives". Electronic Thesis or Diss., Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLY012.
Texto completoMulticomponent reactions play a significant role in organic chemistry. They allow the reaction occur between three or more starting materials, providing adducts which are considered as elements for the syntheses of complex molecules with bioactive compounds. Benifiting from their diversity, these reactions are considered as valuable tools for the preparation of libraries of organic structures in the pharmaceutical research and total synthesis of natural products field.The Passerini reaction, combined with Michael addition and cyclisation, served an easy access to γ-butyrolactones with good yields. The Passerini adducts of aromatic aldehydes act as nucleophiles in Michael additions with acrylonitrile. The reaction proceeds together with hydrolysis of the ester. The resulting γ-hydroxynitrile can be cyclized under acidic conditions to afford γ- butyrolactones.The NH-aryl hydrazones derived from trifluoroacetaldehyde hemiacetal can be involved in efficient Mannich type reactions with formaldehyde and aromatic aldehydes. The resulting hydrazones are useful building blocks for the preparation of trifluoromethyl substituted 1,2-diazine derivatives under heating with β-ketoesters.Moreover, naphthalene derivatives may be obtained through Tsuji-Trost reaction. This reaction may involve the formation of a palladium p-allyl complex followed by a base promoted β-hydride elimination. This reaction combined with the condensation of fused cyclic ketones with nitromethane and the functionalization of the resulting nitrocycloalkenes (Michael, Mannich...) constitute a very powerful synthetic tool for the formation of 1-substituted naphtalenes
Li, Xinghan. "Catalytic strategies designed for precise framework alteration : navigating the uncharted chemical space for drug discovery". Electronic Thesis or Diss., Strasbourg, 2025. http://www.theses.fr/2025STRAF001.
Texto completoWe introduced two programmable strategies to achieve precise skeletal alterations on complex natural products—a progressively divergent ground-up synthesis scheme and a late-stage editing stratagem. Central to the former is the development of a catalytic enantioselective multicomponent process affording a primary hub, transformation of which by a progressively divergent network delivered a scarce alkaloid and its precision skeletal analogs. The linchpin of the latter strategy is the tactical use of olefin metathesis (OM) reactions, including ethenolysis, cross-metathesis, and ring-closing metathesis that are catalyzed by various Ru-, W-, and Mo-complexes. The confluence of OM and other key reactions led us to synthesize an array of skeletally altered epothilone C analogs. In vitro testing, docking, and molecular dynamics validate our approach and justify our contention that precise framework remodeling can lead to the identification of exciting non-natural leads
Dieulle, Laurence. "Fiabilité d'un système de plusieurs groupes de composants avec maintenance à des instants aléatoires". Université de Marne-la-Vallée, 1999. http://www.theses.fr/1999MARN0045.
Texto completoGrassot, Jean-Marie. "Approche vers la synthèse totale de la lipiarmycineUtilisation de para-nitrophénylsulfones dans la réaction de Julia modifiéeSynthèse monotope d'alpha-cétoamides via une nouvelle réaction à quatre composants". Paris 11, 2007. http://www.theses.fr/2007PA112260.
Texto completoThe first part of this thesis was to develop an approach towards the synthesis of lipiarmicin. This macromolecule possesses interesting antibiotic properties and no total synthesis has been already described. Lipiarmicin contains two carbohydrate units and an aglycon. The works presented in this thesis concern the synthesis of the aglycon part which is a 18-membered macrolactone. The formations of five asymmetric centers, two (E),(E) conjugated diene systems and a trisubstitued trans olefin have to be controlled. A strategy based on the elaboration of two principal synthons A and B, has been imagined and explored. Synthons A and B could be connected via a Julia type reaction to build up the trisubstituted olefin and a Yamagushi type macrolactonisation would lead to the desired macrolactone. Thanks to important transformations such as Stille-type couling or Evans aldolisation, we could obtain synthon A and a direct precursor of synthon B. In a second part, and in parallel to the first part, we developed a new version for the modified Julia reaction, which implies the use of para-nitrophenylsulfones. Thanks to this practical method, a library of olefins has been synthesized from aromatic aldehydes with moderate to excellent yields and with good to high stereoselectivities, especially in the case of the fully-stabilised sulfones. In the last part, we described a new synthesis of α-ketoamides based on a four components reaction between an aldehyde, a hydroxylamine, an isonitrile and acetic acid, in presence of molecular sieves. This transformation allowed us to synthesise several ketoamides with different structures, in moderate yields
Sun, Mengfeng. "Analyse qualitative de plusieurs types de systèmes de maladies infectieuses avec effets de réaction ou de diffusion". Thesis, Lille 1, 2019. http://www.theses.fr/2019LIL1I027/document.
Texto completoThis thesis studies some qualitative problems for systems of differential equations modeling in-fectious diseases with reaction or diffusion effects. It consists of three parts.Firstly, we study a complex reaction-diffusion system describing the spatiotemporal spread of in-fluenza with multiple strains. We establish conditions for the existence of semi-, strong and weak (persistent) traveling waves starting from the disease-free equilibrium. We further discuss several situations in which semi-traveling waves do not exist, and give an estimation of minimal wave speed. Secondly, we analyze a class of eco-epidemiological systems where prey is subject to Allee effect and infection. For certain subsystems, we determine the existence of the bifurcation point (Hopf bifurca-tion and bifurcation of heteroclinic orbits). We show that the strong Allee effect can create a separa-trix curve (or surface), leading to multi-stability. We find that the heteroclinic cycles form a hetero-clinic network and identify an interior periodic orbit. Finally, we give a qualitative analysis of two network-based differential systems coupling epidemic spread and information diffusion: the interplay system and the epidemic control system. More specifically, we obtain the existence of the disease-free equilibrium, endemic equilibrium and synchronization manifold, and their global asymptotic stability
Housseman, Christopher. "Synthèse de macrocycles par réaction multi-composants : approche énantiosélective d'une MCR : développement de nouveaux catalyseurs bifonctionnels". Paris 11, 2006. http://www.theses.fr/2006PA112226.
Texto completoBeuvin, Maxime. "Dérivés benzéniques comme composants à deux électrons en cycloadditions : nouveaux processus désaromatisants". Rouen, 2015. http://www.theses.fr/2015ROUES002.
Texto completoAromatic compounds are common and available in large quantities. The dearomatization process is one way to add molecular complexity to these easily accessible compounds. Our group has an interest in the development of new synthetic ways involving cycloaddition reactions to achieve the dearomatization process. It involves electron deficient aromatics as two pi electrons components in a [3+2] or a [4+2] cycloaddition. Our first goal was to use 1,3-dipolar cycloaddition to dearomatize cyanoaromatic derivatives. During this work we found out a new reactivity where the nitrile group undergoes a dipolar cycloaddition with an azomethine ylide. The cycloaddition process proved efficient with a panel of aromatic CN substituted substrates. This reactivity represents a new synthetic route to the imidazoline class of coumpounds and to imidazole derivatives by in situ oxidation of the crude mixture. We also studied the dearomatization of nitroaromatic compounds with a normal-electron demand Diels-Alder reaction using Danishefsky diene. High pressure activation was used to develop this methodology and to improve yields
Bughin, Carine. "Activation d'un acide carboxylique terminal via un oxazole interne : application à la synthèse de cyclodepsipeptides et d'aminosucres cycliques". Paris 11, 2005. http://www.theses.fr/2005PA112265.
Texto completoWe have developed a novel macrolactonization technology. It is a domino process in which a strategically incorporated 5-amino oxazole serves as an internal traceless activator of the neighboring C-terminal carboxylic acid. No coupling reagent is required and the entire sequence is triggered by just a few equivalents of trifluoroacetic acid under very mild conditions. This new methodology has been successfully applied for the synthesis of cyclodepsipeptides and cyclic aminosugars. By combinaison with a three-component synthesis of 5-amino oxazole, a two-step synthesis of structurally complex cyclodepsipeptides, tripeptides and cyclic aminosugars from readily accessible starting materials is developed. An additional study of the mechanism of this domino process has also been provided
Verlut, Isabelle. "Composants cognitifs de l'apprentissage d'habilités : une approche neuropsychologique". Lyon 1, 2000. http://www.theses.fr/2000LYO1T011.
Texto completoCapítulos de libros sobre el tema "Réaction à plusieurs composants"
RIBEIRO, Tony, Maxime FOLSCHETTE, Laurent TRILLING, Nicolas GLADE, Katsumi INOUE, Morgan MAGNIN y Olivier ROUX. "Les enjeux de l’inférence de modèles dynamiques à partir de séries temporelles". En Approches symboliques de la modélisation et de l’analyse des systèmes biologiques, 97–139. ISTE Group, 2022. http://dx.doi.org/10.51926/iste.9029.ch3.
Texto completoSANCHEZ, Samuel. "Les épidémies de choléra-morbus (1831-1852)". En Les épidémies au prisme des SHS, 127–34. Editions des archives contemporaines, 2022. http://dx.doi.org/10.17184/eac.5998.
Texto completoLorre-Johnston, Christine. "Gayatri Chakravorty Spivak". En Gayatri Chakravorty Spivak, 67–87. Hermann, 2023. http://dx.doi.org/10.3917/herm.renau.2023.02.0067.
Texto completoInformes sobre el tema "Réaction à plusieurs composants"
Dolby, G. Palynological analysis of Carboniferous outcrop and corehole samples from the 1993–1995 Magdalen Basin NATMAP Project, with updated data files, locality data, and lists of taxa identified, Prince Edward Island, Nova Scotia, New Brunswick, and Quebec. Natural Resources Canada/CMSS/Information Management, 2024. http://dx.doi.org/10.4095/pcqvf1214e.
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