Academic literature on the topic 'Multicatalyse'

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Journal articles on the topic "Multicatalyse"

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Poe, Sarah L., Muris Kobašlija, and D. Tyler McQuade. "Microcapsule Enabled Multicatalyst System." Journal of the American Chemical Society 128, no. 49 (2006): 15586–87. http://dx.doi.org/10.1021/ja066476l.

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Hofmann, Christine, Sören M. M. Schuler, Raffael C. Wende, and Peter R. Schreiner. "En route to multicatalysis: kinetic resolution of trans-cycloalkane-1,2-diols via oxidative esterification." Chem. Commun. 50, no. 10 (2014): 1221–23. http://dx.doi.org/10.1039/c3cc48584f.

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We demonstrate the application of a multicatalyst to the oxidation of a broad variety of aldehydes and subsequent enantioselective esterification of the incipient acids with (±)-trans-cycloalkane-1,2-diols.
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Mata, José A., F. Ekkehardt Hahn, and Eduardo Peris. "Heterometallic complexes, tandem catalysis and catalytic cooperativity." Chem. Sci. 5, no. 5 (2014): 1723–32. http://dx.doi.org/10.1039/c3sc53126k.

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Ma, Jin-Tao, and Ying Cheng. "Construction of enantiopure imine bridged benzo[c]azepinones by a silver(i) and chiral N-heterocyclic carbene multicatalytic reaction sequence of N′-(2-alkynylbenzylidene)hydrazides and cyclopropanecarbaldehydes." Organic Chemistry Frontiers 7, no. 21 (2020): 3459–67. http://dx.doi.org/10.1039/d0qo00877j.

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Jürjens, Gerrit, Andreas Kirschning, and David A. Candito. "Lessons from the Synthetic Chemist Nature." Natural Product Reports 32, no. 5 (2015): 723–37. http://dx.doi.org/10.1039/c4np00160e.

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Nature's strategy of performing ideal multistep (bio)synthesis are based on multicatalysis, domino reactions, iteration and compartmentation. These are discussed and compared with chemical synthesis in this conceptual review.
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Tang, Xinxin, Lan Gan, Xin Zhang, and Zheng Huang. "n-Alkanes to n-alcohols: Formal primary C─H bond hydroxymethylation via quadruple relay catalysis." Science Advances 6, no. 47 (2020): eabc6688. http://dx.doi.org/10.1126/sciadv.abc6688.

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Nature is able to synergistically combine multiple enzymes to conduct well-ordered biosynthetic transformations. Mimicking nature’s multicatalysis in vitro may give rise to new chemical transformations via interplay of numerous molecular catalysts in one pot. The direct and selective conversion of abundant n-alkanes to valuable n-alcohols is a reaction with enormous potential applicability but has remained an unreached goal. Here, we show that a quadruple relay catalysis system involving three discrete transition metal catalysts enables selective synthesis of n-alcohols via n-alkane primary C─
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Pellissier, Hélène. "Recent developments in enantioselective multicatalysed tandem reactions." Tetrahedron 69, no. 35 (2013): 7171–210. http://dx.doi.org/10.1016/j.tet.2013.06.020.

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Martínez, Sebastián, Lukas Veth, Bruno Lainer, and Paweł Dydio. "Challenges and Opportunities in Multicatalysis." ACS Catalysis 11, no. 7 (2021): 3891–915. http://dx.doi.org/10.1021/acscatal.0c05725.

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Tsoung, Jennifer, Jane Panteleev, Matthias Tesch, and Mark Lautens. "Multicomponent-Multicatalyst Reactions (MC)2R: Efficient Dibenzazepine Synthesis." Organic Letters 16, no. 1 (2013): 110–13. http://dx.doi.org/10.1021/ol4030925.

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Marafi, A., F. Maruyama, A. Stanislaus, and E. Kam. "Multicatalyst System Testing Methodology for Upgrading Residual Oils." Industrial & Engineering Chemistry Research 47, no. 3 (2008): 724–41. http://dx.doi.org/10.1021/ie071103u.

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Dissertations / Theses on the topic "Multicatalyse"

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Hou, Jingke. "Compartmentalized enantioselective multicatalysis using polydimethylsiloxane membrane." Electronic Thesis or Diss., Ecole centrale de Marseille, 2022. http://www.theses.fr/2022ECDM0013.

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Les travaux de cette thèse ont porté sur la production d’énantiomères optiquement enrichis avec une consommation complète du substrat racémiques grâce à un nouveau système compartimenté de double réaction comportant une membrane polydimethylsiloxane (PDMS) à perméabilité sélective.D'abord, la perméabilitéde la membrane PDMS a été étudiée montrant une sélectivité de transfert des espèces en fonction de leur polarité. Par la suite, les réactions opposées d'estérification et de transestérification isolées par une membrane PDMS ont été réalisées pour produire des alcools énantioenrichis séparés à
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Daghmoum, Meriem. "Développement de stratégies multicatalytiques asymétriques : combinaison de la catalyse à l'Au(I) et de la biocatalyse pour la synthèse de molécules chirales." Electronic Thesis or Diss., université Paris-Saclay, 2025. http://www.theses.fr/2025UPASF006.

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La catalyse asymétrique est un outil fondamental pour la synthèse de molécules chirales, indispensables en chimie organique et en pharmacie. Ce travail de thèse explore de nouvelles stratégies impliquant la catalyse à l'Au(I), reconnue pour sa capacité unique à activer les liaisons insaturées et à former des liaisons C-C, C-N ou C-O. Une première partie des travaux s'est concentrée sur le développement de transformations auro-catalysées énantiosélectives, et notamment à leur application dans le développement de réactions de spirocyclisations stéréosélectives en milieu micellaire, ouvrant de no
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Giorgi, Pascal. "Nouvelles réactions à économie d'atomes et d'étapes basées sur la catalyse par des nanoparticules d'or et la multicatalyse. Applications dans la synthèse de chimie fine et des odorants." Thesis, Université Côte d'Azur (ComUE), 2017. http://www.theses.fr/2017AZUR4127.

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L'élaboration de méthodes de synthèse, basées sur l’utilisation d’espèces métalliques a été un sujet de tous les instances en chimie organique. Malgré l’efficacité des métaux utilisés en catalyse homogènes, leurs procédures de recyclage restent limitées. Ce pourquoi, une contrainte supplémentaire a été placée dans la conception de catalyseurs, pouvant offrir à la fois l'efficacité de la catalyse homogène et le recyclage de l’hétérogène. Dans ce contexte, les nanoparticules métalliques sont apparues comme objet phare, en raison de leurs propriétés physico-chimiques inégalées. On a découvert que
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Lainer, Bruno. "A multicatalytic approach to enantio-, and diastereoselective arylation of alcohols." Electronic Thesis or Diss., Strasbourg, 2023. http://www.theses.fr/2023STRAF080.

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Les groupements alcooliques sont présents dans une grande diversité de produits chimiques fins précieux issus de la nature et de la synthèse, c'est pourquoi les méthodes permettant leur diversification structurelle sont recherchées. Cependant, la modification de la structure des alcools à certaines positions non réactives, même avec l'aide de la catalyse, reste un défi ou nécessite des procédures multi-étapes fastidieuses et souvent coûteuses. Récemment, une attention accrue a été accordée à la multicatalyse, qui combine plusieurs catalyseurs au sein d'un même système, ce qui permet de découvr
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Schuler, Sören Manuel Michael [Verfasser]. "(Un)expected extensions of the multicatalysis concept / Sören Manuel Michael Schuler." Gießen : Universitätsbibliothek, 2016. http://d-nb.info/1120270383/34.

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Wende, Raffael Christoph [Verfasser]. "New frontiers in peptide catalysis : multicatalysis, challenging reactions, and the importance of dispersion interactions / Raffael Christoph Wende." Gießen : Universitätsbibliothek, 2016. http://d-nb.info/1114659002/34.

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Kelly, Brendan Douglas. "Part I: Development of New Methods for Multicatalysis: Bismuth(III) Triflate-Catalyzed Hydrofunctionalizations . ." Thesis, 2011. https://doi.org/10.7916/D8SX6M7B.

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This thesis describes the development of novel synthetic methods in two areas of chemical research: Multicatalysis and the aromatic activation of alcohols. The first chapter, encompassing multicatalysis, reveals the design and realization of an innovative hydro-functionalization method. This method is examined in the context of designing multicatalytic processes to access privileged chemical architectures, which unite a nucleophilic addition event with the hydrofunctionalization reaction. The resulting multicatalytic methods capably effect the formation of complex heterocyclic compounds. The s
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Tundel, Rachel E. "I. Multicatalysis: Development of a BiOTf3-catalyzed Nucleophilic Addition/Hydrofunctionalization Reaction in the Synthesis of Complex Heterocycles; . ." Thesis, 2012. https://doi.org/10.7916/D8VX0NV5.

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One of the major drawbacks to traditional syntheses is the requirement for iterative synthesis, which is not only chemically inefficient and time-consuming, but environmentally unfriendly due to waste generated during purification procedures. A way to circumvent problems posed by iterative synthesis is through the development of multicatalytic protocols, in which multiple, distinct synthetic steps can be performed in one reaction pot. Saturated 5-membered oxygen- and nitrogen-containing heterocycles are extremely common structural motifs in many biologically important molecules--a multicatalyt
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Books on the topic "Multicatalyse"

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Pellissier, Hélène. Enantioselective multicatalysed tandem reactions. Royal Soc Of Chemistry, 2014.

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Zhou, Jian, ed. Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.

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Kelly, Brendan Douglas. Part I : Development of New Methods for Multicatalysis: Bismuth Triflate-Catalyzed Hydrofunctionalizations . . . [publisher not identified], 2011.

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Tundel, Rachel E. I. Multicatalysis: Development of a BiOTf3-catalyzed Nucleophilic Addition/Hydrofunctionalization Reaction in the Synthesis of Complex Heterocycles; . . . [publisher not identified], 2012.

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Enantioselective Multicatalysed Tandem Reactions. Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/9781782621355.

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Enantioselective Multicatalysed Tandem Reactions. Royal Society of Chemistry, The, 2014.

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Enantioselective Multicatalysed Tandem Reactions. Royal Society of Chemistry, The, 2014.

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Zhou, Jian. Multicatalyst System in Asymmetric Catalysis. Wiley, 2014.

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Zhou, Jian. Multicatalyst System in Asymmetric Catalysis. Wiley & Sons, Incorporated, John, 2014.

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Zhou, Jian. Multicatalyst System in Asymmetric Catalysis. Wiley & Sons, Incorporated, John, 2014.

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Book chapters on the topic "Multicatalyse"

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Cao, Zhong-Yan, Feng Zhu, and Jian Zhou. "Multicatalyst System." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch2.

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Zeng, Xing-Ping, and Jian Zhou. "Asymmetric Assisted Catalysis by Multicatalyst System." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch6.

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Zhou, Feng, Yun-Lin Liu, and Jian Zhou. "Multicatalyst System Realized Asymmetric Tandem Reactions." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch8.

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Zhou, Jian, and Jin-Sheng Yu. "Toward Ideal Asymmetric Catalysis." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch1.

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Liu, Yun-Lin, and Jian Zhou. "Multicatalyst System Mediated Asymmetric Reactions in Total Synthesis." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch10.

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Yu, Jin-Sheng, and Jian Zhou. "Asymmetric Multifunctional Catalysis." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch3.

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Chen, Long, Yun-Lin Liu, and Jian Zhou. "Asymmetric Cooperative Catalysis." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch4.

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Chen, Long, Zhong-Yan Cao, and Jian Zhou. "Asymmetric Double Activation Catalysis by Multicatalyst System." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch5.

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Cao, Zhong-Yan, and Jian Zhou. "Asymmetric Catalysis Facilitated by Photochemical or Electrochemical Methods." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch7.

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Zhou, Jian, and Xing-Ping Zeng. "Waste-Mediated Reactions." In Multicatalyst System in Asymmetric Catalysis. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118846919.ch9.

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