Artigos de revistas sobre o tema "Multicatalysis"
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Martínez, Sebastián, Lukas Veth, Bruno Lainer e Paweł Dydio. "Challenges and Opportunities in Multicatalysis". ACS Catalysis 11, n.º 7 (15 de março de 2021): 3891–915. http://dx.doi.org/10.1021/acscatal.0c05725.
Texto completo da fonteMa, Jin-Tao, e 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, n.º 21 (2020): 3459–67. http://dx.doi.org/10.1039/d0qo00877j.
Texto completo da fonteJürjens, Gerrit, Andreas Kirschning e David A. Candito. "Lessons from the Synthetic Chemist Nature". Natural Product Reports 32, n.º 5 (2015): 723–37. http://dx.doi.org/10.1039/c4np00160e.
Texto completo da fonteTang, Xinxin, Lan Gan, Xin Zhang e Zheng Huang. "n-Alkanes to n-alcohols: Formal primary C─H bond hydroxymethylation via quadruple relay catalysis". Science Advances 6, n.º 47 (novembro de 2020): eabc6688. http://dx.doi.org/10.1126/sciadv.abc6688.
Texto completo da fonteSancheti, Shashank P., Urvashi, Mosami P. Shah e Nitin T. Patil. "Ternary Catalysis: A Stepping Stone toward Multicatalysis". ACS Catalysis 10, n.º 5 (8 de janeiro de 2020): 3462–89. http://dx.doi.org/10.1021/acscatal.9b04000.
Texto completo da fonteAmbrosini, Lisa M., e Tristan H. Lambert. "Multicatalysis: Advancing Synthetic Efficiency and Inspiring Discovery". ChemCatChem 2, n.º 11 (17 de setembro de 2010): 1373–80. http://dx.doi.org/10.1002/cctc.200900323.
Texto completo da fonteJindal, Garima, e Raghavan B. Sunoj. "Mechanistic Insights on Cooperative Asymmetric Multicatalysis Using Chiral Counterions". Journal of Organic Chemistry 79, n.º 16 (29 de julho de 2014): 7600–7606. http://dx.doi.org/10.1021/jo501322v.
Texto completo da fonteKim, Mahn-Joo, Min Young Choi, Min Young Han, Yoon Kyung Choi, Jae Kwan Lee e Jaiwook Park. "Asymmetric Transformations of Acyloxyphenyl Ketones by Enzyme−Metal Multicatalysis". Journal of Organic Chemistry 67, n.º 26 (dezembro de 2002): 9481–83. http://dx.doi.org/10.1021/jo026122m.
Texto completo da fonteAmbrosini, Lisa M., e Tristan H. Lambert. "ChemInform Abstract: Multicatalysis: Advancing Synthetic Efficiency and Inspiring Discovery". ChemInform 42, n.º 9 (3 de fevereiro de 2011): no. http://dx.doi.org/10.1002/chin.201109248.
Texto completo da fonteShugrue, Christopher R., Bianca R. Sculimbrene, Elizabeth R. Jarvo, Brandon Q. Mercado e Scott J. Miller. "Outer-Sphere Control for Divergent Multicatalysis with Common Catalytic Moieties". Journal of Organic Chemistry 84, n.º 3 (4 de janeiro de 2019): 1664–72. http://dx.doi.org/10.1021/acs.joc.8b03068.
Texto completo da fonteRichmond, Edward, Ismat Ullah Khan e Joseph Moran. "Enantioselective and Regiodivergent Functionalization ofN-Allylcarbamates by Mechanistically Divergent Multicatalysis". Chemistry - A European Journal 22, n.º 35 (27 de julho de 2016): 12274–77. http://dx.doi.org/10.1002/chem.201602792.
Texto completo da fonteHofmann, Christine, Sören M. M. Schuler, Raffael C. Wende e Peter R. Schreiner. "En route to multicatalysis: kinetic resolution of trans-cycloalkane-1,2-diols via oxidative esterification". Chem. Commun. 50, n.º 10 (2014): 1221–23. http://dx.doi.org/10.1039/c3cc48584f.
Texto completo da fonteXiao, Pin, Haiyan Yuan, Jianquan Liu, Yiying Zheng, Xihe Bi e Jingping Zhang. "Radical Mechanism of Isocyanide-Alkyne Cycloaddition by Multicatalysis of Ag2CO3, Solvent, and Substrate". ACS Catalysis 5, n.º 10 (22 de setembro de 2015): 6177–84. http://dx.doi.org/10.1021/acscatal.5b01703.
Texto completo da fonteGeorgi, Anett, Miriam Velasco Polo, Klara Crincoli, Katrin Mackenzie e Frank-Dieter Kopinke. "Accelerated Catalytic Fenton Reaction with Traces of Iron: An Fe–Pd-Multicatalysis Approach". Environmental Science & Technology 50, n.º 11 (26 de maio de 2016): 5882–91. http://dx.doi.org/10.1021/acs.est.6b01049.
Texto completo da fonteYoun, So Won, Hyoung Sub Song e Jong Hyub Park. "Asymmetric Domino Multicatalysis for the Synthesis of 3-Substituted Phthalides: Cinchonine/NHC Cooperative System". Organic Letters 16, n.º 3 (24 de janeiro de 2014): 1028–31. http://dx.doi.org/10.1021/ol5000617.
Texto completo da fonteLorion, Mélanie M., Nikolaos Kaplaneris, Jongwoo Son, Rositha Kuniyil e Lutz Ackermann. "Late‐Stage Peptide Diversification through Cobalt‐Catalyzed C−H Activation: Sequential Multicatalysis for Stapled Peptides". Angewandte Chemie 131, n.º 6 (9 de janeiro de 2019): 1698–702. http://dx.doi.org/10.1002/ange.201811668.
Texto completo da fonteRamachary, Dhevalapally B., Rumpa Mondal e Chintalapudi Venkaiah. "Rapid Synthesis of Functionalized Indenes, Triazoles, and Glucocorticoid Receptor Modulators by Sequential Multicatalysis Cascade Reactions". European Journal of Organic Chemistry 2010, n.º 17 (3 de maio de 2010): 3205–10. http://dx.doi.org/10.1002/ejoc.201000220.
Texto completo da fonteLorion, Mélanie M., Nikolaos Kaplaneris, Jongwoo Son, Rositha Kuniyil e Lutz Ackermann. "Late‐Stage Peptide Diversification through Cobalt‐Catalyzed C−H Activation: Sequential Multicatalysis for Stapled Peptides". Angewandte Chemie International Edition 58, n.º 6 (9 de janeiro de 2019): 1684–88. http://dx.doi.org/10.1002/anie.201811668.
Texto completo da fonteBreder, Alexander, e Christian Depken. "Light‐Driven Single‐Electron Transfer Processes as an Enabling Principle in Sulfur and Selenium Multicatalysis". Angewandte Chemie International Edition 58, n.º 48 (25 de novembro de 2019): 17130–47. http://dx.doi.org/10.1002/anie.201812486.
Texto completo da fonteJin, Zhichao, Jianfeng Xu, Song Yang, Bao-An Song e Yonggui Robin Chi. "Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N-Heterocyclic-Carbene/Thiourea/Tertiary-Amine Multicatalysis". Angewandte Chemie 125, n.º 47 (2 de outubro de 2013): 12580–84. http://dx.doi.org/10.1002/ange.201305023.
Texto completo da fonteHofmann, Christine, Soeren M. M. Schuler, Raffael C. Wende e Peter R. Schreiner. "ChemInform Abstract: En route to Multicatalysis: Kinetic Resolution of trans-Cycloalkane-1,2-diols via Oxidative Esterification." ChemInform 45, n.º 22 (15 de maio de 2014): no. http://dx.doi.org/10.1002/chin.201422067.
Texto completo da fonteYoun, So Won, Hyoung Sub Song e Jong Hyub Park. "ChemInform Abstract: Asymmetric Domino Multicatalysis for the Synthesis of 3-Substituted Phthalides: Cinchonine/NHC Cooperative System." ChemInform 45, n.º 29 (3 de julho de 2014): no. http://dx.doi.org/10.1002/chin.201429125.
Texto completo da fonteJin, Zhichao, Jianfeng Xu, Song Yang, Bao-An Song e Yonggui Robin Chi. "Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N-Heterocyclic-Carbene/Thiourea/Tertiary-Amine Multicatalysis". Angewandte Chemie International Edition 52, n.º 47 (2 de outubro de 2013): 12354–58. http://dx.doi.org/10.1002/anie.201305023.
Texto completo da fonteRamachary, Dhevalapally B., Rumpa Mondal e Chintalapudi Venkaiah. "ChemInform Abstract: Rapid Synthesis of Functionalized Indenes, Triazoles, and Glucocorticoid Receptor Modulators by Sequential Multicatalysis Cascade Reactions." ChemInform 41, n.º 44 (7 de outubro de 2010): no. http://dx.doi.org/10.1002/chin.201044036.
Texto completo da fonteLiu, Jiahui, Yiying Zheng, Ying Liu, Haiyan Yuan e Jingping Zhang. "Mechanistic insight on (E )-methyl 3-(2-aminophenyl)acrylate cyclization reaction by multicatalysis of solvent and substrate". Journal of Computational Chemistry 37, n.º 26 (4 de agosto de 2016): 2386–94. http://dx.doi.org/10.1002/jcc.24463.
Texto completo da fonteJin, Zhichao, Jianfeng Xu, Song Yang, Bao-An Song e Yonggui Robin Chi. "ChemInform Abstract: Enantioselective Sulfonation of Enones with Sulfonyl Imines by Cooperative N-Heterocyclic-Carbene/Thiourea/Tertiary-Amine Multicatalysis." ChemInform 45, n.º 14 (21 de março de 2014): no. http://dx.doi.org/10.1002/chin.201414093.
Texto completo da fontePaul, Jérôme, Tania Xavier, Marc Presset, Erwan Le Gall, Eric Léonel, Christophe Pichon e Sylvie Condon. "Cobalt-Zinc-Diimine Multicatalysis: Enhanced syn Diastereoselectivity in the Reductive Multicomponent Coupling of Aryl Bromides, Acrylates and Aldehydes". ChemistrySelect 3, n.º 47 (18 de dezembro de 2018): 13480–86. http://dx.doi.org/10.1002/slct.201803710.
Texto completo da fonteSanchez Díaz-Marta, Antonio, Susana Yáñez, Carmen R. Tubío, V. Laura Barrio, Yolanda Piñeiro, Rosa Pedrido, José Rivas, Manuel Amorín, Francisco Guitián e Alberto Coelho. "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, n.º 28 (21 de junho de 2019): 25283–94. http://dx.doi.org/10.1021/acsami.9b08119.
Texto completo da fonteJúnior, Aldo Araújo da Trindade, Yan Ferraz Ximenes Ladeira, Alexandre da Silva França, Rodrigo Octavio Mendonça Alves de Souza, Adolfo Henrique Moraes, Robert Wojcieszak, Ivaldo Itabaiana Jr. e Amanda Silva de Miranda. "Multicatalytic Hybrid Materials for Biocatalytic and Chemoenzymatic Cascades—Strategies for Multicatalyst (Enzyme) Co-Immobilization". Catalysts 11, n.º 8 (31 de julho de 2021): 936. http://dx.doi.org/10.3390/catal11080936.
Texto completo da fonteSakthivel, Shanmugam, e 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, n.º 19 (4 de setembro de 2018): 12171–83. http://dx.doi.org/10.1021/acs.joc.8b02127.
Texto completo da fonteRamachary, Dhevalapally B., Kinthada Ramakumar, Adluri Bharanishashank e 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, n.º 6 (8 de novembro de 2010): 855–76. http://dx.doi.org/10.1021/cc100104k.
Texto completo da fonteMata, José A., F. Ekkehardt Hahn e Eduardo Peris. "Heterometallic complexes, tandem catalysis and catalytic cooperativity". Chem. Sci. 5, n.º 5 (2014): 1723–32. http://dx.doi.org/10.1039/c3sc53126k.
Texto completo da fonteGaur, Akshay, Chirag Porwal, Imed Boukhris, Vishal Singh Chauhan e Rahul Vaish. "Review on Multicatalytic Behavior of Ba0.85Ca0.15Ti0.9Zr0.1O3 Ceramic". Materials 16, n.º 16 (21 de agosto de 2023): 5710. http://dx.doi.org/10.3390/ma16165710.
Texto completo da fonteArribas, J., M. Luz Rodríguez, R. Alvarez-Do Forno e J. G. Castaño. "Autoantibodies against the multicatalytic proteinase in patients with systemic lupus erythematosus." Journal of Experimental Medicine 173, n.º 2 (1 de fevereiro de 1991): 423–27. http://dx.doi.org/10.1084/jem.173.2.423.
Texto completo da fonteRivett, A. J. "The Multicatalytic Proteinase". Journal of Biological Chemistry 264, n.º 21 (julho de 1989): 12215–19. http://dx.doi.org/10.1016/s0021-9258(18)63843-8.
Texto completo da fonteNelson, Judith E., Claudia Altschuller-Felberg, Anna Loukissa e Christopher Cardozo. "Proteasome from cytokine-treated human cells shows stimulated BrAAP activity and depressed PGPH activity". Biochemistry and Cell Biology 78, n.º 2 (1 de abril de 2000): 115–18. http://dx.doi.org/10.1139/o00-006.
Texto completo da fonteRivett, A. J. "Proteasomes: multicatalytic proteinase complexes". Biochemical Journal 291, n.º 1 (1 de abril de 1993): 1–10. http://dx.doi.org/10.1042/bj2910001.
Texto completo da fonteHo, Xuan-Huong, Won-Ji Jung, Pranab K. Shyam e Hye-Young Jang. "Copper–dienamine catalysis: γ-oxyamination of α,β-unsaturated aldehydes". Catal. Sci. Technol. 4, n.º 7 (2014): 1914–19. http://dx.doi.org/10.1039/c4cy00271g.
Texto completo da fontePoe, Sarah L., Muris Kobašlija e D. Tyler McQuade. "Microcapsule Enabled Multicatalyst System". Journal of the American Chemical Society 128, n.º 49 (dezembro de 2006): 15586–87. http://dx.doi.org/10.1021/ja066476l.
Texto completo da fonteZhang, Xiao-Qian, Xue-Jiao Lv, Jun-Ping Pei, Rui Tan e 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, n.º 2 (2020): 292–97. http://dx.doi.org/10.1039/c9qo01272a.
Texto completo da fonteWagner, B. J., Joyce W. Margolis e Inderpal Singh. "Bovine Lens Multicatalytic Proteinase Complex". Enzyme and Protein 47, n.º 4-6 (1993): 202–9. http://dx.doi.org/10.1159/000468679.
Texto completo da fonteFolco, Eduardo J., Liliana Busconi, Celina B. Martone e Jorge J. Sanchez. "Multicatalytic proteinase in fish muscle". Archives of Biochemistry and Biophysics 267, n.º 2 (dezembro de 1988): 599–605. http://dx.doi.org/10.1016/0003-9861(88)90067-7.
Texto completo da fonteS�nchez, Jorge J., Eduardo J. Folco, Liliana Busconi, Celina B. Martone, Claudia Studdert e Claudia A. Casalongu�. "Multicatalytic proteinase in fish muscle". Molecular Biology Reports 21, n.º 1 (1995): 63–69. http://dx.doi.org/10.1007/bf00990973.
Texto completo da fonteSAVORY, PETER J., e A. JENNIFER RIVETT. "Catalytic subunits of the multicatalytic proteinase". Biochemical Society Transactions 19, n.º 3 (1 de agosto de 1991): 292S. http://dx.doi.org/10.1042/bst019292s.
Texto completo da fonteELLISON, DEREK S., JOHN HINTON e ROBERT J. BEYNON. "Construction of an artificial ‘multicatalytic protease’". Biochemical Society Transactions 21, n.º 1 (1 de fevereiro de 1993): 33S. http://dx.doi.org/10.1042/bst021033s.
Texto completo da fonteNOTHWANG, Hans-Gred, Oliver COUX, Faycal BEY e Klaus SCHERRER. "Prosomes and their multicatalytic proteinase activity". European Journal of Biochemistry 207, n.º 2 (julho de 1992): 621–30. http://dx.doi.org/10.1111/j.1432-1033.1992.tb17089.x.
Texto completo da fonteEleuteri, Anna Maria, Ronald A. Kohanski, Christopher Cardozo e Marian Orlowski. "Bovine Spleen Multicatalytic Proteinase Complex (Proteasome)". Journal of Biological Chemistry 272, n.º 18 (2 de maio de 1997): 11824–31. http://dx.doi.org/10.1074/jbc.272.18.11824.
Texto completo da fonteZein, Haggag S., Jaime A. Teixeira da Silva e Kazutaka Miyatake. "Molecular analysis of multicatalytic monoclonal antibodies". Molecular Immunology 47, n.º 9 (maio de 2010): 1747–56. http://dx.doi.org/10.1016/j.molimm.2010.02.024.
Texto completo da fonteRechsteiner, M., L. Hoffman e W. Dubiel. "The multicatalytic and 26 S proteases." Journal of Biological Chemistry 268, n.º 9 (março de 1993): 6065–68. http://dx.doi.org/10.1016/s0021-9258(18)53218-x.
Texto completo da fonteSWEENEY, SEAN T., e A. JENNIFER RIVETT. "Immunological properties of the multicatalytic proteinase". Biochemical Society Transactions 17, n.º 6 (1 de dezembro de 1989): 1126–27. http://dx.doi.org/10.1042/bst0171126.
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