Увійти

Готові списки джерел за темами / Multicatalysis / Статті в журналах

Статті в журналах з теми "Multicatalysis"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Multicatalysis.

Автор: Grafiati

Опубліковано: 25 травня 2024

Оновлено: 7 липня 2024

Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями

Оберіть тип джерела:

Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Multicatalysis".

Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.

Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.

Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.

1

Martínez, Sebastián, Lukas Veth, Bruno Lainer, and Paweł Dydio. "Challenges and Opportunities in Multicatalysis." ACS Catalysis 11, no. 7 (March 15, 2021): 3891–915. http://dx.doi.org/10.1021/acscatal.0c05725.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (November 2020): eabc6688. http://dx.doi.org/10.1126/sciadv.abc6688.

Повний текст джерела

Анотація:

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─H bond hydroxymethylation. This one-pot multicatalysis system is composed of Ir-catalyzed alkane dehydrogenation, Rh-catalyzed olefin isomerization and hydroformylation, and Ru-catalyzed aldehyde hydrogenation. This system is further applied to synthesis of α,ω-diols from simple α-olefins through terminal-selective hydroxymethylation of silyl alkanes.

Стилі APA, Harvard, Vancouver, ISO та ін.

5

Sancheti, Shashank P., Urvashi, Mosami P. Shah, and Nitin T. Patil. "Ternary Catalysis: A Stepping Stone toward Multicatalysis." ACS Catalysis 10, no. 5 (January 8, 2020): 3462–89. http://dx.doi.org/10.1021/acscatal.9b04000.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

6

Ambrosini, Lisa M., and Tristan H. Lambert. "Multicatalysis: Advancing Synthetic Efficiency and Inspiring Discovery." ChemCatChem 2, no. 11 (September 17, 2010): 1373–80. http://dx.doi.org/10.1002/cctc.200900323.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

7

Jindal, Garima, and Raghavan B. Sunoj. "Mechanistic Insights on Cooperative Asymmetric Multicatalysis Using Chiral Counterions." Journal of Organic Chemistry 79, no. 16 (July 29, 2014): 7600–7606. http://dx.doi.org/10.1021/jo501322v.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (December 2002): 9481–83. http://dx.doi.org/10.1021/jo026122m.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

9

Ambrosini, Lisa M., and Tristan H. Lambert. "ChemInform Abstract: Multicatalysis: Advancing Synthetic Efficiency and Inspiring Discovery." ChemInform 42, no. 9 (February 3, 2011): no. http://dx.doi.org/10.1002/chin.201109248.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (January 4, 2019): 1664–72. http://dx.doi.org/10.1021/acs.joc.8b03068.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (July 27, 2016): 12274–77. http://dx.doi.org/10.1002/chem.201602792.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (September 22, 2015): 6177–84. http://dx.doi.org/10.1021/acscatal.5b01703.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (May 26, 2016): 5882–91. http://dx.doi.org/10.1021/acs.est.6b01049.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (January 24, 2014): 1028–31. http://dx.doi.org/10.1021/ol5000617.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (January 9, 2019): 1698–702. http://dx.doi.org/10.1002/ange.201811668.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (May 3, 2010): 3205–10. http://dx.doi.org/10.1002/ejoc.201000220.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (January 9, 2019): 1684–88. http://dx.doi.org/10.1002/anie.201811668.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (November 25, 2019): 17130–47. http://dx.doi.org/10.1002/anie.201812486.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (October 2, 2013): 12580–84. http://dx.doi.org/10.1002/ange.201305023.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (May 15, 2014): no. http://dx.doi.org/10.1002/chin.201422067.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (July 3, 2014): no. http://dx.doi.org/10.1002/chin.201429125.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (October 2, 2013): 12354–58. http://dx.doi.org/10.1002/anie.201305023.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (October 7, 2010): no. http://dx.doi.org/10.1002/chin.201044036.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (August 4, 2016): 2386–94. http://dx.doi.org/10.1002/jcc.24463.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (March 21, 2014): no. http://dx.doi.org/10.1002/chin.201414093.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

27

Paul, Jérôme, Tania Xavier, Marc Presset, Erwan Le Gall, Eric Léonel, Christophe Pichon, and Sylvie Condon. "Cobalt-Zinc-Diimine Multicatalysis: Enhanced syn Diastereoselectivity in the Reductive Multicomponent Coupling of Aryl Bromides, Acrylates and Aldehydes." ChemistrySelect 3, no. 47 (December 18, 2018): 13480–86. http://dx.doi.org/10.1002/slct.201803710.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

28

Sanchez Díaz-Marta, Antonio, Susana Yáñez, Carmen R. Tubío, V. Laura Barrio, Yolanda Piñeiro, Rosa Pedrido, José Rivas, Manuel Amorín, Francisco Guitián, and 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, no. 28 (June 21, 2019): 25283–94. http://dx.doi.org/10.1021/acsami.9b08119.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

29

Júnior, 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., and Amanda Silva de Miranda. "Multicatalytic Hybrid Materials for Biocatalytic and Chemoenzymatic Cascades—Strategies for Multicatalyst (Enzyme) Co-Immobilization." Catalysts 11, no. 8 (July 31, 2021): 936. http://dx.doi.org/10.3390/catal11080936.

Повний текст джерела

Анотація:

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 solution to these problems. This review gives an overview of all the pathways for enzyme immobilization and their use in integrated enzymatic and chemoenzymatic processes in cascade or in a one-pot concomitant execution. We place emphasis on the factors that must be considered to understand the process of immobilization. A better understanding of this fundamental process is an essential tool not only in the choice of the best route of immobilization but also in the understanding of their catalytic activity.

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (September 4, 2018): 12171–83. http://dx.doi.org/10.1021/acs.joc.8b02127.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (November 8, 2010): 855–76. http://dx.doi.org/10.1021/cc100104k.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (August 21, 2023): 5710. http://dx.doi.org/10.3390/ma16165710.

Повний текст джерела

Анотація:

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 applications. It also highlights the fundamentals of ferroelectric ceramics, the importance of electric poling, and the principles underlying piezocatalysis, photocatalysis, and pyrocatalysis processes in addition to the multicatalytic capability of ferroelectric BCZTO ceramic.

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (February 1, 1991): 423–27. http://dx.doi.org/10.1084/jem.173.2.423.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

35

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

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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 (April 1, 2000): 115–18. http://dx.doi.org/10.1139/o00-006.

Повний текст джерела

Анотація:

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 conclusion that the increased BrAAP activity of LMP-containing multicatalytic proteinase complex results from incorporation of LMP7 or other LMP subunits.

Стилі APA, Harvard, Vancouver, ISO та ін.

37

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

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

39

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

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

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.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

41

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.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

42

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 (December 1988): 599–605. http://dx.doi.org/10.1016/0003-9861(88)90067-7.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

43

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.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

44

SAVORY, PETER J., and A. JENNIFER RIVETT. "Catalytic subunits of the multicatalytic proteinase." Biochemical Society Transactions 19, no. 3 (August 1, 1991): 292S. http://dx.doi.org/10.1042/bst019292s.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

45

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

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

46

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

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

47

Eleuteri, Anna Maria, Ronald A. Kohanski, Christopher Cardozo, and Marian Orlowski. "Bovine Spleen Multicatalytic Proteinase Complex (Proteasome)." Journal of Biological Chemistry 272, no. 18 (May 2, 1997): 11824–31. http://dx.doi.org/10.1074/jbc.272.18.11824.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

48

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

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

49

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

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

50

SWEENEY, SEAN T., and A. JENNIFER RIVETT. "Immunological properties of the multicatalytic proteinase." Biochemical Society Transactions 17, no. 6 (December 1, 1989): 1126–27. http://dx.doi.org/10.1042/bst0171126.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

Ми пропонуємо знижки на всі преміум-плани для авторів, чиї праці увійшли до тематичних добірок літератури. Зв'яжіться з нами, щоб отримати унікальний промокод!