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Artículos de revistas sobre el tema "Multicatalysis"

Autor: Grafiati
Publicado: 25 de mayo de 2024
Última modificación: 31 de julio de 2025

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1

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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2

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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3

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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4

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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5

Sancheti, Shashank P., Urvashi, Mosami P. Shah, and Nitin T. Patil. "Ternary Catalysis: A Stepping Stone toward Multicatalysis." ACS Catalysis 10, no. 5 (2020): 3462–89. http://dx.doi.org/10.1021/acscatal.9b04000.

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6

Ambrosini, Lisa M., and Tristan H. Lambert. "Multicatalysis: Advancing Synthetic Efficiency and Inspiring Discovery." ChemCatChem 2, no. 11 (2010): 1373–80. http://dx.doi.org/10.1002/cctc.200900323.

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7

Jindal, Garima, and Raghavan B. Sunoj. "Mechanistic Insights on Cooperative Asymmetric Multicatalysis Using Chiral Counterions." Journal of Organic Chemistry 79, no. 16 (2014): 7600–7606. http://dx.doi.org/10.1021/jo501322v.

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8

Kim, Mahn-Joo, Min Young Choi, Min Young Han, Yoon Kyung Choi, Jae Kwan Lee, and Jaiwook Park. "Asymmetric Transformations of Acyloxyphenyl Ketones by Enzyme−Metal Multicatalysis." Journal of Organic Chemistry 67, no. 26 (2002): 9481–83. http://dx.doi.org/10.1021/jo026122m.

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9

Ambrosini, Lisa M., and Tristan H. Lambert. "ChemInform Abstract: Multicatalysis: Advancing Synthetic Efficiency and Inspiring Discovery." ChemInform 42, no. 9 (2011): no. http://dx.doi.org/10.1002/chin.201109248.

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10

Shugrue, Christopher R., Bianca R. Sculimbrene, Elizabeth R. Jarvo, Brandon Q. Mercado, and Scott J. Miller. "Outer-Sphere Control for Divergent Multicatalysis with Common Catalytic Moieties." Journal of Organic Chemistry 84, no. 3 (2019): 1664–72. http://dx.doi.org/10.1021/acs.joc.8b03068.

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11

Richmond, Edward, Ismat Ullah Khan, and Joseph Moran. "Enantioselective and Regiodivergent Functionalization ofN-Allylcarbamates by Mechanistically Divergent Multicatalysis." Chemistry - A European Journal 22, no. 35 (2016): 12274–77. http://dx.doi.org/10.1002/chem.201602792.

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12

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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13

Xiao, Pin, Haiyan Yuan, Jianquan Liu, Yiying Zheng, Xihe Bi, and Jingping Zhang. "Radical Mechanism of Isocyanide-Alkyne Cycloaddition by Multicatalysis of Ag2CO3, Solvent, and Substrate." ACS Catalysis 5, no. 10 (2015): 6177–84. http://dx.doi.org/10.1021/acscatal.5b01703.

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14

Georgi, Anett, Miriam Velasco Polo, Klara Crincoli, Katrin Mackenzie, and Frank-Dieter Kopinke. "Accelerated Catalytic Fenton Reaction with Traces of Iron: An Fe–Pd-Multicatalysis Approach." Environmental Science & Technology 50, no. 11 (2016): 5882–91. http://dx.doi.org/10.1021/acs.est.6b01049.

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15

Youn, So Won, Hyoung Sub Song, and Jong Hyub Park. "Asymmetric Domino Multicatalysis for the Synthesis of 3-Substituted Phthalides: Cinchonine/NHC Cooperative System." Organic Letters 16, no. 3 (2014): 1028–31. http://dx.doi.org/10.1021/ol5000617.

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16

Lorion, Mélanie M., Nikolaos Kaplaneris, Jongwoo Son, Rositha Kuniyil, and Lutz Ackermann. "Late‐Stage Peptide Diversification through Cobalt‐Catalyzed C−H Activation: Sequential Multicatalysis for Stapled Peptides." Angewandte Chemie 131, no. 6 (2019): 1698–702. http://dx.doi.org/10.1002/ange.201811668.

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17

Ramachary, Dhevalapally B., Rumpa Mondal, and Chintalapudi Venkaiah. "Rapid Synthesis of Functionalized Indenes, Triazoles, and Glucocorticoid Receptor Modulators by Sequential Multicatalysis Cascade Reactions." European Journal of Organic Chemistry 2010, no. 17 (2010): 3205–10. http://dx.doi.org/10.1002/ejoc.201000220.

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18

Lorion, Mélanie M., Nikolaos Kaplaneris, Jongwoo Son, Rositha Kuniyil, and Lutz Ackermann. "Late‐Stage Peptide Diversification through Cobalt‐Catalyzed C−H Activation: Sequential Multicatalysis for Stapled Peptides." Angewandte Chemie International Edition 58, no. 6 (2019): 1684–88. http://dx.doi.org/10.1002/anie.201811668.

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19

Breder, Alexander, and Christian Depken. "Light‐Driven Single‐Electron Transfer Processes as an Enabling Principle in Sulfur and Selenium Multicatalysis." Angewandte Chemie International Edition 58, no. 48 (2019): 17130–47. http://dx.doi.org/10.1002/anie.201812486.

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20

Jin, Zhichao, Jianfeng Xu, Song Yang, Bao-An Song, and Yonggui Robin Chi. "Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N-Heterocyclic-Carbene/Thiourea/Tertiary-Amine Multicatalysis." Angewandte Chemie 125, no. 47 (2013): 12580–84. http://dx.doi.org/10.1002/ange.201305023.

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21

Hofmann, Christine, Soeren M. M. Schuler, Raffael C. Wende, and Peter R. Schreiner. "ChemInform Abstract: En route to Multicatalysis: Kinetic Resolution of trans-Cycloalkane-1,2-diols via Oxidative Esterification." ChemInform 45, no. 22 (2014): no. http://dx.doi.org/10.1002/chin.201422067.

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22

Youn, So Won, Hyoung Sub Song, and Jong Hyub Park. "ChemInform Abstract: Asymmetric Domino Multicatalysis for the Synthesis of 3-Substituted Phthalides: Cinchonine/NHC Cooperative System." ChemInform 45, no. 29 (2014): no. http://dx.doi.org/10.1002/chin.201429125.

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23

Jin, Zhichao, Jianfeng Xu, Song Yang, Bao-An Song, and Yonggui Robin Chi. "Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N-Heterocyclic-Carbene/Thiourea/Tertiary-Amine Multicatalysis." Angewandte Chemie International Edition 52, no. 47 (2013): 12354–58. http://dx.doi.org/10.1002/anie.201305023.

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24

Ramachary, Dhevalapally B., Rumpa Mondal, and Chintalapudi Venkaiah. "ChemInform Abstract: Rapid Synthesis of Functionalized Indenes, Triazoles, and Glucocorticoid Receptor Modulators by Sequential Multicatalysis Cascade Reactions." ChemInform 41, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.201044036.

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25

Liu, Jiahui, Yiying Zheng, Ying Liu, Haiyan Yuan, and Jingping Zhang. "Mechanistic insight on (E )-methyl 3-(2-aminophenyl)acrylate cyclization reaction by multicatalysis of solvent and substrate." Journal of Computational Chemistry 37, no. 26 (2016): 2386–94. http://dx.doi.org/10.1002/jcc.24463.

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26

Jin, Zhichao, Jianfeng Xu, Song Yang, Bao-An Song, and Yonggui Robin Chi. "ChemInform Abstract: Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N-Heterocyclic-Carbene/Thiourea/Tertiary-Amine Multicatalysis." ChemInform 45, no. 14 (2014): no. http://dx.doi.org/10.1002/chin.201414093.

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27

Paul, Jérôme, Tania Xavier, Marc Presset, et al. "Cobalt-Zinc-Diimine Multicatalysis: Enhanced syn Diastereoselectivity in the Reductive Multicomponent Coupling of Aryl Bromides, Acrylates and Aldehydes." ChemistrySelect 3, no. 47 (2018): 13480–86. http://dx.doi.org/10.1002/slct.201803710.

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28

Sanchez Díaz-Marta, Antonio, Susana Yáñez, Carmen R. Tubío, et al. "Multicatalysis Combining 3D-Printed Devices and Magnetic Nanoparticles in One-Pot Reactions: Steps Forward in Compartmentation and Recyclability of Catalysts." ACS Applied Materials & Interfaces 11, no. 28 (2019): 25283–94. http://dx.doi.org/10.1021/acsami.9b08119.

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29

Júnior, Aldo Araújo da Trindade, Yan Ferraz Ximenes Ladeira, Alexandre da Silva França, et al. "Multicatalytic Hybrid Materials for Biocatalytic and Chemoenzymatic Cascades—Strategies for Multicatalyst (Enzyme) Co-Immobilization." Catalysts 11, no. 8 (2021): 936. http://dx.doi.org/10.3390/catal11080936.

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During recent decades, the use of enzymes or chemoenzymatic cascades for organic chemistry has gained much importance in fundamental and industrial research. Moreover, several enzymatic and chemoenzymatic reactions have also served in green and sustainable manufacturing processes especially in fine chemicals, pharmaceutical, and flavor/fragrance industries. Unfortunately, only a few processes have been applied at industrial scale because of the low stabilities of enzymes along with the problematic processes of their recovery and reuse. Immobilization and co-immobilization offer an ideal soluti
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30

Sakthivel, Shanmugam, and Rengarajan Balamurugan. "Annulation of a Highly Functionalized Diazo Building Block with Indoles under Sc(OTf)3/Rh2(OAc)4 Multicatalysis through Michael Addition/Cyclization Sequence." Journal of Organic Chemistry 83, no. 19 (2018): 12171–83. http://dx.doi.org/10.1021/acs.joc.8b02127.

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31

Ramachary, Dhevalapally B., Kinthada Ramakumar, Adluri Bharanishashank, and Vidadala V. Narayana. "Sequential One-Pot Combination of Multireactions through Multicatalysis: A General Approach to Rapid Assembly of Functionalized Push−Pull Olefins, Phenols, and 2-Methyl-2H-chromenes." Journal of Combinatorial Chemistry 12, no. 6 (2010): 855–76. http://dx.doi.org/10.1021/cc100104k.

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32

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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33

Gaur, Akshay, Chirag Porwal, Imed Boukhris, Vishal Singh Chauhan, and Rahul Vaish. "Review on Multicatalytic Behavior of Ba0.85Ca0.15Ti0.9Zr0.1O3 Ceramic." Materials 16, no. 16 (2023): 5710. http://dx.doi.org/10.3390/ma16165710.

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Ferroelectric materials are known to possess multicatalytic abilities that are nowadays utilized for removing organic pollutants from water via piezocatalysis, photocatalysis, piezo-photocatalysis, and pyrocatalysis processes. The Ba0.85Ca0.15Ti0.9Zr0.1O3 (BCZTO) ceramic is one such ferroelectric composition that has been extensively studied for electrical and electronic applications. Furthermore, the BCZTO ceramic has also shown remarkable multicatalytic performance in water-cleaning applications. The present review explores the potentiality of BCZTO for water-cleaning and bacterial-killing a
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34

Arribas, J., M. Luz Rodríguez, R. Alvarez-Do Forno, and J. G. Castaño. "Autoantibodies against the multicatalytic proteinase in patients with systemic lupus erythematosus." Journal of Experimental Medicine 173, no. 2 (1991): 423–27. http://dx.doi.org/10.1084/jem.173.2.423.

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Sera from patients with systemic lupus erythematosus contain specific autoantibodies directed against different polypeptide components of the multicatalytic proteinase (also known as proteasome or prosome). These human autoantibodies, in contrast to polyclonal antibodies obtained in rabbits against the purified enzyme, recognize highly conserved epitopes of the multicatalytic proteinase polypeptides from yeast to human.
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35

Rivett, A. J. "The Multicatalytic Proteinase." Journal of Biological Chemistry 264, no. 21 (1989): 12215–19. http://dx.doi.org/10.1016/s0021-9258(18)63843-8.

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36

Nelson, Judith E., Claudia Altschuller-Felberg, Anna Loukissa, and Christopher Cardozo. "Proteasome from cytokine-treated human cells shows stimulated BrAAP activity and depressed PGPH activity." Biochemistry and Cell Biology 78, no. 2 (2000): 115–18. http://dx.doi.org/10.1139/o00-006.

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The branched chain amino acid-preferring (BrAAP) activity of multicatalytic proteinase complex isolated from human umbilical vein endothelial cells and treated with interferon-gamma was increased more than 2-fold, which was associated with a marked increase in LMP7 expression and decreased peptidylglutamyl peptide-hydrolyzing activity. Increases in BrAAP activity in supernatants from cells treated with interferon-gamma, tumor necrosis factor-alpha, interleukin-1beta, interleukin-6, or lipopolysaccharide paralleled the increases in LMP7 expression. These findings are consistent with the conclus
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37

Rivett, A. J. "Proteasomes: multicatalytic proteinase complexes." Biochemical Journal 291, no. 1 (1993): 1–10. http://dx.doi.org/10.1042/bj2910001.

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38

Ho, Xuan-Huong, Won-Ji Jung, Pranab K. Shyam та Hye-Young Jang. "Copper–dienamine catalysis: γ-oxyamination of α,β-unsaturated aldehydes". Catal. Sci. Technol. 4, № 7 (2014): 1914–19. http://dx.doi.org/10.1039/c4cy00271g.

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39

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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40

Zhang, Xiao-Qian, Xue-Jiao Lv, Jun-Ping Pei, Rui Tan, and Yan-Kai Liu. "An asymmetric multicatalytic reaction sequence of 2-hydroxycinnamaldehydes and enolic 1,3-dicarbonyl compounds to construct bridged bicyclic acetals." Organic Chemistry Frontiers 7, no. 2 (2020): 292–97. http://dx.doi.org/10.1039/c9qo01272a.

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2-Hydroxycinnamaldehydes and cyclic 1,3-dicarbonyl nucleophiles were used in an asymmetric organocatalyzed reaction sequence to construct bridged bicyclic acetals via a multicatalytic process involving iminium catalysis and anion-binding catalysis.
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41

Fernandes, Antony E., and Alain M. Jonas. "Design of Multicatalytic Systems Through Self-Assembly." Catalysts 15, no. 3 (2025): 265. https://doi.org/10.3390/catal15030265.

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The development of self-assembled multicatalytic systems has emerged as a promising strategy for mimicking enzymatic catalysis in synthetic systems. This approach leverages the use of non-covalent interactions, such as hydrophobic interactions, hydrogen bonding, metal–ligand coordination, and aromatic stacking, to organize multiple catalytic centers within a defined, cooperative framework, allowing for enhanced reactivity, selectivity and efficiency, akin to the behavior of natural enzymes. The versatility of this approach enables the modular design, preparation, screening and optimization of
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42

Wagner, B. J., Joyce W. Margolis, and Inderpal Singh. "Bovine Lens Multicatalytic Proteinase Complex." Enzyme and Protein 47, no. 4-6 (1993): 202–9. http://dx.doi.org/10.1159/000468679.

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43

Folco, Eduardo J., Liliana Busconi, Celina B. Martone, and Jorge J. Sanchez. "Multicatalytic proteinase in fish muscle." Archives of Biochemistry and Biophysics 267, no. 2 (1988): 599–605. http://dx.doi.org/10.1016/0003-9861(88)90067-7.

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44

S�nchez, Jorge J., Eduardo J. Folco, Liliana Busconi, Celina B. Martone, Claudia Studdert, and Claudia A. Casalongu�. "Multicatalytic proteinase in fish muscle." Molecular Biology Reports 21, no. 1 (1995): 63–69. http://dx.doi.org/10.1007/bf00990973.

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45

SAVORY, PETER J., and A. JENNIFER RIVETT. "Catalytic subunits of the multicatalytic proteinase." Biochemical Society Transactions 19, no. 3 (1991): 292S. http://dx.doi.org/10.1042/bst019292s.

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46

ELLISON, DEREK S., JOHN HINTON, and ROBERT J. BEYNON. "Construction of an artificial ‘multicatalytic protease’." Biochemical Society Transactions 21, no. 1 (1993): 33S. http://dx.doi.org/10.1042/bst021033s.

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47

NOTHWANG, Hans-Gred, Oliver COUX, Faycal BEY, and Klaus SCHERRER. "Prosomes and their multicatalytic proteinase activity." European Journal of Biochemistry 207, no. 2 (1992): 621–30. http://dx.doi.org/10.1111/j.1432-1033.1992.tb17089.x.

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48

Eleuteri, Anna Maria, Ronald A. Kohanski, Christopher Cardozo, and Marian Orlowski. "Bovine Spleen Multicatalytic Proteinase Complex (Proteasome)." Journal of Biological Chemistry 272, no. 18 (1997): 11824–31. http://dx.doi.org/10.1074/jbc.272.18.11824.

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49

Zein, Haggag S., Jaime A. Teixeira da Silva, and Kazutaka Miyatake. "Molecular analysis of multicatalytic monoclonal antibodies." Molecular Immunology 47, no. 9 (2010): 1747–56. http://dx.doi.org/10.1016/j.molimm.2010.02.024.

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50

Rechsteiner, M., L. Hoffman, and W. Dubiel. "The multicatalytic and 26 S proteases." Journal of Biological Chemistry 268, no. 9 (1993): 6065–68. http://dx.doi.org/10.1016/s0021-9258(18)53218-x.

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