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Literatura académica sobre el tema "Cycle taille moyenne"
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Artículos de revistas sobre el tema "Cycle taille moyenne"
Boly, Hamidou, L. Magagi, T. Konaté, M. C. Viguier Martinez y A. Yenikoye. "Cycle oestral et croissance folliculaire de la brebis Djallonké variété "Mossi"". Revue d’élevage et de médecine vétérinaire des pays tropicaux 45, n.º 3-4 (1 de marzo de 1992): 335–40. http://dx.doi.org/10.19182/remvt.8928.
Texto completoLebourgeois, François. "Le blaireau européen (Meles meles L.). Synthèse des connaissances européennes. Partie 2 : groupes familiaux, dynamiques des populations et domaines vitaux". Revue forestière française 72, n.º 2 (30 de abril de 2020): 99–118. http://dx.doi.org/10.20870/revforfr.2020.5313.
Texto completoEdmond Fulgence, Thiemelle Deless, Koffi Eric-Blanchard Zadjéhi, Issali Auguste Emmanuel, Kouame Tchrewa Stanislas y Gnonhouri Philippe. "Évaluation de la Variabilité Génétique d’Une Collection de Bananiers Plantain (Musa sp.) Cultivés en Côte d’Ivoire à Partir d’Une Caractérisation Agro-morphologique". European Scientific Journal, ESJ 18, n.º 40 (31 de diciembre de 2022): 366. http://dx.doi.org/10.19044/esj.2022.v18n40p366.
Texto completoMonteil, Karine y Annie-H. Rouard. "Influence de la taille des «plaquettes» sur les paramètres biomécaniques du crawl". STAPS 13, n.º 27 (1992): 31–40. http://dx.doi.org/10.3406/staps.1992.895.
Texto completoDjagba, Atouga Yembliman, Bèdibètè Bonfoh, Habrè Bassowa, Kodjo Aklikokou y N’gonlbi Kanour. "Etat des lieux de l’élevage caprin en milieu paysan au Togo". Revue d’élevage et de médecine vétérinaire des pays tropicaux 73, n.º 1 (28 de febrero de 2020): 11–19. http://dx.doi.org/10.19182/remvt.31840.
Texto completoDiaw, O. T., M. Seye y Y. Sarr. "Résistance à la sécheresse de mollusques du genre <em> Bulinus </em> vecteurs de trématodoses humaines et animales au Sénégal. II. Etude dans les conditions naturelles en zone Nord-soudanienne. Ecologie et résistance à la sécheresse de <em> Bulinus umbilicatus </em> et <em> B. sene </em>". Revue d’élevage et de médecine vétérinaire des pays tropicaux 42, n.º 2 (1 de febrero de 1989): 177–87. http://dx.doi.org/10.19182/remvt.8827.
Texto completoVEYSSET, P., M. LHERM y D. BEBIN. "Évolutions, dispersions et déterminants du revenu en élevage bovin allaitant charolais. Etude sur 15 ans (1989-2003) à partir d’un échantillon constant de 69 exploitations". INRAE Productions Animales 18, n.º 4 (18 de octubre de 2005): 265–75. http://dx.doi.org/10.20870/productions-animales.2005.18.4.3532.
Texto completoChiurdoglu, G., R. De Proost y B. Tursch. "Cycles de Taille Moyenne II. Spectres infra-rouges de cyclanes monosubstitués". Bulletin des Sociétés Chimiques Belges 67, n.º 5-6 (1 de septiembre de 2010): 198–203. http://dx.doi.org/10.1002/bscb.19580670505.
Texto completoALI MOUSSA, Aïssatou, Aimé Christian NDIH y Madi ALI. "Typologie des élevages de lapins dans la zone sahélienne du Cameroun : cas de la ville de Maroua". Journal of Applied Biosciences 185 (31 de mayo de 2023): 19393–401. http://dx.doi.org/10.35759/jabs.185.3.
Texto completoChiurdoglu, G., R. Fuks y B. Tursch. "Cycles de Taille Moyenne I. Etudes conformationnelles en série cyclodécanique a l'aide de l'hypothèse de Prelog". Bulletin des Sociétés Chimiques Belges 67, n.º 5-6 (1 de septiembre de 2010): 191–97. http://dx.doi.org/10.1002/bscb.19580670504.
Texto completoTesis sobre el tema "Cycle taille moyenne"
Dousset, Maxime. "Réaction d'expansion de cycle : études dirigées vers l'accès aux cycles de taille moyenne via des espèces polarisées". Thesis, Aix-Marseille, 2017. http://www.theses.fr/2017AIXM0577.
Texto completoIn the quest for new therapeutic candidates, the description of novel synthetic approaches to access to increasingly complex carbon systems remains a daunting challenge. In order to increase the structural of such scaffolds, it is necessary to overcome the encountered difficulties by developing new straightforward an efficient tools. In this context, this work has mainly focused on the access of structurally defined carbon cycles by ring expansion reactions via the use of polarized compounds. The first part of this study has been devoted to the Tiffeneau-Demjanov ring expansion reaction using ethyl α-chlorodiazoacetate. This approach allowed us to access highly versatile cyclic keto esters displaying a tetrasubstitued carbon center bearing a chlorine atom. The next topic of this study has been focused on the development of a (5 + 3) cycloaddition reaction between two polarized cyclopropane entities. This methodology led to the description of a novel reactivity of donor-acceptor cyclopropanes compounds to form α,β,γ-trisubstituted lactones under a BrØnsted acid activation. In order to gain mechanistic insights, a theoretical study has also been conducted which led us to rationalize the mechanism and the selectivity of this transformation. The last part described the reactivity of a underexplored class of molecule, the vinylbiscyclopropanes. These compound, can lead to the benzocyclobutene family and to the 8 membered-ring compounds through rearrangement or formal [3.3] sigmatropic rearrangement reaction. This last class of compound is still under study and should allow rapid access to diverse cyclic structures
Dousset, Maxime. "Réaction d'expansion de cycle : études dirigées vers l'accès aux cycles de taille moyenne via des espèces polarisées". Electronic Thesis or Diss., Aix-Marseille, 2017. http://www.theses.fr/2017AIXM0577.
Texto completoIn the quest for new therapeutic candidates, the description of novel synthetic approaches to access to increasingly complex carbon systems remains a daunting challenge. In order to increase the structural of such scaffolds, it is necessary to overcome the encountered difficulties by developing new straightforward an efficient tools. In this context, this work has mainly focused on the access of structurally defined carbon cycles by ring expansion reactions via the use of polarized compounds. The first part of this study has been devoted to the Tiffeneau-Demjanov ring expansion reaction using ethyl α-chlorodiazoacetate. This approach allowed us to access highly versatile cyclic keto esters displaying a tetrasubstitued carbon center bearing a chlorine atom. The next topic of this study has been focused on the development of a (5 + 3) cycloaddition reaction between two polarized cyclopropane entities. This methodology led to the description of a novel reactivity of donor-acceptor cyclopropanes compounds to form α,β,γ-trisubstituted lactones under a BrØnsted acid activation. In order to gain mechanistic insights, a theoretical study has also been conducted which led us to rationalize the mechanism and the selectivity of this transformation. The last part described the reactivity of a underexplored class of molecule, the vinylbiscyclopropanes. These compound, can lead to the benzocyclobutene family and to the 8 membered-ring compounds through rearrangement or formal [3.3] sigmatropic rearrangement reaction. This last class of compound is still under study and should allow rapid access to diverse cyclic structures
Divay, Mathilde. "De l'identification d'un processus de developpement a la specification de l'entreprise de taille moyenne : une approche par la theorie du cycle de vie". Caen, 1999. http://www.theses.fr/1999CAEN0584.
Texto completoThe identification of the middle sized organization as an intermediate firm asks the question of the enterprise's development process. The research of useful concepts in order to help the understanding of the firm's development can be implemented through a transversal approach to the management science, with the using of biological analogy. The evolutionary theory of the firm also integrate the life cycle theory as a level of observation of the organization development. It allows then a better understanding of its components. A model is then developed which study the dynamic relation between age, size and rate of growth of the firm. It is tested on a population of 1427 firms in basse- normandie with the integration of qualitative variables. Different behaviour can be found between growing-stage firms and maturity stage firms
De, Dobbeleer Corinne. "Synthèse de cycles de taille moyenne fonctionnalisés". Université catholique de Louvain, 2005. http://edoc.bib.ucl.ac.be:81/ETD-db/collection/available/BelnUcetd-10042005-091150/.
Texto completoMasson, Kevin. "Synthèse thermique de composés carbocycliques à huit chaînons supportée par calculs DFT". Electronic Thesis or Diss., Aix-Marseille, 2022. http://www.theses.fr/2022AIXM0461.
Texto completoEight-membered carbocyclic systems are widely represented motifs in natural and bio-active molecules. However, they remain under-represented in both marketed drugs and in drug discovery programs. This is mostly due to the well-known challenge of making them, due to the inherent ring strain. On the other hand, small rings represent a valuable three-atoms building element in the search to reach molecular complexity in an atom economical manner and often participate in fascinating chemical transformations. This release of ring tension usually allows for a scalable, rapid and controlled synthetic access to the expected target molecules. In this context, a new class of donor-acceptor cyclopropane (DAC) has recently been developed in the laboratory combining a silyl protected cyclopropanol with an α,β-unsaturated ester. Gratifyingly, the latter delivered polyfunctionalized cyclooctadienes in good yields in purely thermal conditions. The experiments ran in the laboratory demonstrated that the thermal rearrangement of DACs is totally regioselective and highly diastereoselective. A small library of highly substituted cyclooctanoïds was obtained without the need of any reagent nor transition metals. Finally, mechanistic investigations performed on selected DACs allowed us to better understand the course of the reaction and highlighted the formation of highly reactive trans-cyclooctadienes as intermediates, known for their high and unusual reactivity
"Synthèse de cycles de taille moyenne fonctionnalisés". Université catholique de Louvain, 2005. http://edoc.bib.ucl.ac.be:81/ETD-db/collection/available/BelnUcetd-10042005-091150/.
Texto completo