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Добірка наукової літератури з теми "Amide fonction"
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Статті в журналах з теми "Amide fonction"
Deprez, Dominique, Rodolphe Margraff, Jean Bizot, and Jean-Pierre Pulicani. "Reduction electrochimique de la fonction amide d'un compose antitumoral, l'echinosporine." Tetrahedron Letters 28, no. 40 (January 1987): 4679–80. http://dx.doi.org/10.1016/s0040-4039(00)96595-x.
Повний текст джерелаLaguerre, A., J. C. Rabadeux, H. Gueniffey та C. M. Bruneau. "Fixation d'acides α aminés sur chaînes méthacryliques par l'intermédiaire d'une fonction amide". European Polymer Journal 23, № 11 (січень 1987): 851–53. http://dx.doi.org/10.1016/0014-3057(87)90057-7.
Повний текст джерелаPilichowski, J. F., J. M. Lehn, J. P. Sauvage, and J. C. Gramain. "Synthese de coordinats macrocycliques polyazotes comportant une fonction amine secondaire discriminee." Tetrahedron 41, no. 10 (January 1985): 1959–64. http://dx.doi.org/10.1016/s0040-4020(01)96560-3.
Повний текст джерелаSimon, E., A. Périchaud, P. Bernier, and S. Lefrant. "Fonctionnalisation du (CH)x ex PVC : greffage de fonction amine aromatique." Journal de Chimie Physique 89 (1992): 1257–62. http://dx.doi.org/10.1051/jcp/1992891257.
Повний текст джерелаMontheard, J. P., J. M. Vergnaud, and N. Chafi. "Hydrolyses de polymeres acryliques et methacryliques porteurs de fonctions amides." European Polymer Journal 25, no. 11 (January 1989): 1103–11. http://dx.doi.org/10.1016/0014-3057(89)90165-1.
Повний текст джерелаAbarbri, Mohamed, Alain Guignard, and Maurice Lamant. "Les ?-c�tonitriles groupes protecteurs de la fonction amine. Pr�paration d'amino-alcools." Helvetica Chimica Acta 78, no. 1 (February 8, 1995): 109–21. http://dx.doi.org/10.1002/hlca.19950780111.
Повний текст джерелаGrenier-Loustalot, Marie-Florence, F. Cazaux, J. Berecoechea, and P. Grenier. "Réactivité du groupement époxyde vis à vis d'une amine aromatique en fonction de l'environnement moléculaire." European Polymer Journal 22, no. 6 (January 1986): 471–80. http://dx.doi.org/10.1016/0014-3057(86)90008-x.
Повний текст джерелаHoualla, Douraid, Zouhair Bounja, Marie-carmen Monje, and Saïd Skouta. "EXTENSION DE LA RÉACTION DE TODD AUX 1-HYDRIDO-1-ORGANYLOXYBICYCLO-PHOSPHORANES PORTEURS D'UNE FONCTION AMINE SECONDAIRE." Phosphorus, Sulfur, and Silicon and the Related Elements 81, no. 1-4 (January 1993): 1–15. http://dx.doi.org/10.1080/10426509308034369.
Повний текст джерелаLe Rudulier, M., C. Moinet та E. Raoult. "Préparation de cations [η5-cyclopentadiényl fer η6-arène]+ comportant une fonction oxime, cétone, amine ou alcool en α du ligande arène". Journal of Organometallic Chemistry 310, № 2 (серпень 1986): 209–24. http://dx.doi.org/10.1016/s0022-328x(00)99554-8.
Повний текст джерелаLe Rudulier, M., та C. Moinet. "Prèparation de cations chiraux (η5-cyclopentadiènyl fer η6-arène)+ comportant une fonction oxime ou cètone en α du ligande arène, réduction électrochimique en amine ou en alcool optiquement actifs". Journal of Organometallic Chemistry 352, № 3 (вересень 1988): 337–55. http://dx.doi.org/10.1016/0022-328x(88)83123-1.
Повний текст джерелаДисертації з теми "Amide fonction"
Berthon, Claude. "Etude par rmn de la conformation des extractants a fonction amide en phase organique." Clermont-Ferrand 2, 1993. http://www.theses.fr/1993CLF21481.
Повний текст джерелаTosi, Eleonora. "Nouvelles opportunités pour la synthèse peptidique." Electronic Thesis or Diss., Montpellier, Ecole nationale supérieure de chimie, 2022. http://www.theses.fr/2022ENCM0008.
Повний текст джерелаPeptides and proteins are amongst the essential molecules in the everyday life. Consequently, they are widely investigated and used in several synthetic and natural-derived materials covering a broad range of applications. Hence, mastering their production, especially by chemical synthesis, is of utmost importance.Our group has proposed an original procedure for the formation of amides on the basis of a novel mode of activation (“inverse activation” of AA through the amine function) affording the synthesis of several dipeptides. Nonetheless, this methodology presents some main drawbacks such as the long time to complete the reaction.This PhD thesis work focuses on improving this methodology to synthesise peptide targets and to be able to extend the methodology to the synthesis of “general” (no-amino acids substrates) amides. To accomplish our aim, we examined the different parameters of the peptide coupling such as the solvent, the concentration, the activating reagent, the additives and the time of the reaction. For instance, in terms of reaction kinetics we were delighted to observe that the reaction could take place in only 30 minutes instead of 20 hours using microwave irradiation. Moreover, we found that the additives used for the reaction (CuBr2/HOBt 10 mol% each) could be replaced by a catalytic amount of trifluoroacetic acid in a more diluted solution to give dipeptides in good yield (in the absence of a transition metal). Then, we focus our attention on the synthesis of general amides. Once the reaction conditions were optimised, we explored the scope of the substrate obtaining the desired products in good yield showing the versatility of this methodology.In parallel, we realised another project on the ring-expansion of the vinyl aziridines in order to afford the formation of 3-pyrrolines, interesting building blocks in organic synthesis
TOULEMONDE, VALERIE. "Cinetique d'extraction liquide-liquide du nitrate d'uranyle et des nitrates d'actinides (iii) et des lanthanides (iii) par des extractants a fonction amide." Paris 6, 1995. http://www.theses.fr/1995PA066742.
Повний текст джерелаHoller, Michel. "Reactifs chromophoriques des fonctions thiol et amine." Strasbourg 1, 1994. http://www.theses.fr/1994STR13196.
Повний текст джерелаRACAPE, EVELYNE. "Influence des fonctions amides sur les proprietes physicochimiques des pectines." Nantes, 1989. http://www.theses.fr/1989NANT2001.
Повний текст джерелаBrière, Jean-François. "Elaboration d'une enzyme artificielle se liant à des fonctions amines et des fonctions acides dans le but de catalyser la formation de liaisons amides." Rouen, 1998. http://www.theses.fr/1998ROUES097.
Повний текст джерелаMercier, Nathalie. "Expression, régulation et fonctions de la "semicarbazide-sensitive amine oxidase" (SSAO) dans le tissu adipeux et la paroi vasculaire." Paris 6, 2003. http://www.theses.fr/2003PA066218.
Повний текст джерелаDupret, Isabelle. "Contribution à l'étude de la biodégradation de modèles et de polymères contenant des fonctions esters et amides ou uréthannes." Doctoral thesis, Universite Libre de Bruxelles, 1998. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/212033.
Повний текст джерелаLaval, Stéphane. "Nouveaux systèmes réducteurs utilisant des hydrosiloxanes comme substituts des hydrures d’aluminium et de bore : application à la réduction des fonctions amides et nitriles." Thesis, Lyon 1, 2011. http://www.theses.fr/2011LYO10193/document.
Повний текст джерелаIn recent years, industrial and academic researches have experienced unprecedented changes related to the concept of sustainable development. Health and environment new requirements have prompted chemists to develop chemical products and processes that reduce or eliminate hazardous substances. The research work described in this thesis is focused on the development of new reducing systems using hydrosiloxanes as substitutes for aluminum and boron hydrides. In order to achieve this goal, reducing systems combining 1,1,3,3-tetramethyldisiloxane (TMDS) or polymethylhydrosiloxane (PMHS) with titanium or vanadium complexes have been developed for the reduction of amides and nitriles. The nature of both the association “hydrosiloxane – metal” as well as the studied substrate played an important role on the performance and the selectivity of the reaction. On the one hand, selective reductions of amides (tertiary and secondary) and nitriles to aldehydes were carried out respectively in the presence of titanium(IV) tetraisopropoxide and vanadium(V) triisopropoxide oxide. On the other hand, reductions of amides (primary) and nitriles afforded the corresponding primary amines in the presence of titanium(IV) tetraisopropoxide. Finally, these systems have been applied for the synthesis of saturated N-heterocycles. Reduction of dinitrile compounds led, in one step, to piperidine, pyrrolidine and azetidine derivatives through an intramolecular reductive alkylation reaction
Guignard, Alain. "Emploi de la cyano-2 cyclopentanone comme agent de blocage de la fonction amine, synthèse d'amino-alcools optiquement actifs application à la préparation d'oxazolines chirales." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37598106b.
Повний текст джерелаКниги з теми "Amide fonction"
Storme, Marcel, and P. van Orshoven. Amice curiae, quo vadis?: Het openbaar ministerie in privaatrechtelijke, administratieve en sociale zaken = le ministère public en matière civile, commerciale, administrative et sociale. Edited by Centre interuniversitaire de droit judiciaire. Antwerpen: Kluwer, 2002.
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