Статті в журналах з теми "Reductive reactions"
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Koóš, Peter, Martin Markovič, Pavol Lopatka, and Tibor Gracza. "Recent Applications of Continuous Flow in Homogeneous Palladium Catalysis." Synthesis 52, no. 23 (August 3, 2020): 3511–29. http://dx.doi.org/10.1055/s-0040-1707212.
Повний текст джерелаNicholas, Kenneth M., and Chandrasekhar Bandari. "Deoxygenative Transition-Metal-Promoted Reductive Coupling and Cross-Coupling of Alcohols and Epoxides." Synthesis 53, no. 02 (October 7, 2020): 267–78. http://dx.doi.org/10.1055/s-0040-1707269.
Повний текст джерелаDutta, Lona, Atanu Mondal, and S. S. V. Ramasastry. "Metal‐Free Reductive Aldol Reactions." Asian Journal of Organic Chemistry 10, no. 4 (March 10, 2021): 680–91. http://dx.doi.org/10.1002/ajoc.202000693.
Повний текст джерелаPal, Sudipta, You-Yun Zhou, and Christopher Uyeda. "Catalytic Reductive Vinylidene Transfer Reactions." Journal of the American Chemical Society 139, no. 34 (August 17, 2017): 11686–89. http://dx.doi.org/10.1021/jacs.7b05901.
Повний текст джерелаLin, Ivan J. B., Hayder A. Zahalka, and Howard Alper. "Rhodium catalyzed reductive esterification reactions." Tetrahedron Letters 29, no. 15 (January 1988): 1759–62. http://dx.doi.org/10.1016/s0040-4039(00)82035-3.
Повний текст джерелаAnderson, James C., Alexander J. Blake, Paul J. Koovits, and Gregory J. Stepney. "Diastereoselective Reductive Nitro-Mannich Reactions." Journal of Organic Chemistry 77, no. 10 (May 2, 2012): 4711–24. http://dx.doi.org/10.1021/jo300535h.
Повний текст джерелаWerth, Jacob, Kristen Berger, and Christopher Uyeda. "Cobalt Catalyzed Reductive Spirocyclopropanation Reactions." Advanced Synthesis & Catalysis 362, no. 2 (November 22, 2019): 348–52. http://dx.doi.org/10.1002/adsc.201901293.
Повний текст джерелаWang, Zhipeng A., Yan-Yu Liang, and Ji-Shen Zheng. "Reductive Amination/Alkylation Reactions: The Recent Developments, Progresses, and Applications in Protein Chemical Biology Studies." Current Organic Synthesis 15, no. 6 (August 29, 2018): 755–61. http://dx.doi.org/10.2174/1570179415666180522093905.
Повний текст джерелаPaterson, Lorna A., Sandra E. Hill, John R. Mitchell, and John M. V. Blanshard. "Sulphite and oxidative—reductive depolymerization reactions." Food Chemistry 60, no. 2 (October 1997): 143–47. http://dx.doi.org/10.1016/s0308-8146(95)00253-7.
Повний текст джерелаDonohoe, Timothy J., Karl W. Ace, Paul M. Guyo, Madeleine Helliwell, and Jeffrey McKenna. "Reductive aldol reactions on aromatic heterocycles." Tetrahedron Letters 41, no. 7 (February 2000): 989–93. http://dx.doi.org/10.1016/s0040-4039(99)02224-8.
Повний текст джерелаHawkins, Bill C., Paul A. Keller, and Stephen G. Pyne. "Reductive ring opening reactions of diphenyldihydrofullerenylpyrroles." Tetrahedron Letters 48, no. 42 (October 2007): 7533–36. http://dx.doi.org/10.1016/j.tetlet.2007.08.044.
Повний текст джерелаPanfilov, A. V., Yu D. Markovich, I. P. Ivashev, A. A. Zhirov, A. F. Eleev, V. K. Kurochkin, A. T. Kirsanov, and G. V. Nazarov. "Sodium borohydride in reductive amination reactions." Pharmaceutical Chemistry Journal 34, no. 2 (February 2000): 76–78. http://dx.doi.org/10.1007/bf02524364.
Повний текст джерелаBochkarev, M. N., and L. V. Pankratov. "Principles of oxidative-reductive transmetallation reactions." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, no. 8 (August 1987): 1717–22. http://dx.doi.org/10.1007/bf00960141.
Повний текст джерелаCadoux, Cécile, and Ross D. Milton. "Recent Enzymatic Electrochemistry for Reductive Reactions." ChemElectroChem 7, no. 9 (April 2, 2020): 1974–86. http://dx.doi.org/10.1002/celc.202000282.
Повний текст джерелаWu, Hongli, Shuo-Qing Zhang, and Xin Hong. "Mechanisms of nickel-catalyzed reductive cross-coupling reactions." Chemical Synthesis 3, no. 4 (2023): 39. http://dx.doi.org/10.20517/cs.2023.20.
Повний текст джерелаZhou, You-Yun, and Christopher Uyeda. "Catalytic reductive [4 + 1]-cycloadditions of vinylidenes and dienes." Science 363, no. 6429 (February 21, 2019): 857–62. http://dx.doi.org/10.1126/science.aau0364.
Повний текст джерелаWang, Yuling, and Qinghua Ren. "DFT Study of the Mechanisms of Transition-Metal-Catalyzed Reductive Coupling Reactions." Current Organic Chemistry 24, no. 12 (September 22, 2020): 1367–83. http://dx.doi.org/10.2174/1385272824999200608135840.
Повний текст джерелаValdés, Carlos, Miguel Paraja, and Manuel Plaza. "Transition-Metal-Free Reactions Between Boronic Acids and N-Sulfonylhydrazones or Diazo Compounds: Reductive Coupling Processes and Beyond." Synlett 28, no. 18 (August 22, 2017): 2373–89. http://dx.doi.org/10.1055/s-0036-1590868.
Повний текст джерелаShu, Xing-Zhong, Xiaobo Pang, and Xuejing Peng. "Reductive Cross-Coupling of Vinyl Electrophiles." Synthesis 52, no. 24 (August 11, 2020): 3751–63. http://dx.doi.org/10.1055/s-0040-1707342.
Повний текст джерелаRietveld, Patrick, L. David Arscott, Alan Berry, Nigel S. Scrutton, Mahendra P. Deonarain, Richard N. Perham, and Charles H. Williams. "Reductive and Oxidative Half-Reactions of Glutathione Reductase from Escherichia coli." Biochemistry 33, no. 46 (November 1994): 13888–95. http://dx.doi.org/10.1021/bi00250a043.
Повний текст джерелаMitsudome, Takato. "Air-Stable and Highly Active Transition Metal Phosphide Catalysts for Reductive Molecular Transformations." Catalysts 14, no. 3 (March 12, 2024): 193. http://dx.doi.org/10.3390/catal14030193.
Повний текст джерелаSarhan, Abd El-Wareth A. O. "[4 + 3]Cycloaddition Reactions: Synthesis of 9,10-Dimethoxy-9,10-propanoanthracen-12-ones." Journal of Chemical Research 23, no. 1 (January 1999): 24–25. http://dx.doi.org/10.1177/174751989902300118.
Повний текст джерелаMikesell, Peter, Michael Schwaebe, Marcello DiMare, R. Daniel Little, Giuseppe Silvestri, André Tallec, Tatsuya Shono, and H. Toftlund. "Electrochemical Reductive Coupling Reactions of Aliphatic Nitroalkenes." Acta Chemica Scandinavica 53 (1999): 792–99. http://dx.doi.org/10.3891/acta.chem.scand.53-0792.
Повний текст джерелаTortajada, Andreu, Marino Börjesson, and Ruben Martin. "Nickel-Catalyzed Reductive Carboxylation and Amidation Reactions." Accounts of Chemical Research 54, no. 20 (September 29, 2021): 3941–52. http://dx.doi.org/10.1021/acs.accounts.1c00480.
Повний текст джерелаNozawa-Kumada, Kanako, Shungo Ito, Koto Noguchi, Masanori Shigeno, and Yoshinori Kondo. "Super electron donor-mediated reductive desulfurization reactions." Chemical Communications 55, no. 86 (2019): 12968–71. http://dx.doi.org/10.1039/c9cc06775b.
Повний текст джерелаPoremba, Kelsey E., Sara E. Dibrell, and Sarah E. Reisman. "Nickel-Catalyzed Enantioselective Reductive Cross-Coupling Reactions." ACS Catalysis 10, no. 15 (June 24, 2020): 8237–46. http://dx.doi.org/10.1021/acscatal.0c01842.
Повний текст джерелаZhao, Gui-Ling, and Armando Córdova. "Direct organocatalytic asymmetric reductive Mannich-type reactions." Tetrahedron Letters 47, no. 42 (October 2006): 7417–21. http://dx.doi.org/10.1016/j.tetlet.2006.08.063.
Повний текст джерелаKlatte, Stephanie, Elisabeth Lorenz, and Volker F. Wendisch. "Whole cell biotransformation for reductive amination reactions." Bioengineered 5, no. 1 (December 5, 2013): 56–62. http://dx.doi.org/10.4161/bioe.27151.
Повний текст джерелаPolidoro, Daniele, Daily Rodriguez-Padron, Alvise Perosa, Rafael Luque, and Maurizio Selva. "Chitin-Derived Nanocatalysts for Reductive Amination Reactions." Materials 16, no. 2 (January 6, 2023): 575. http://dx.doi.org/10.3390/ma16020575.
Повний текст джерелаAnderson, James C., Alexander J. Blake, Paul J. Koovits, and Gregory J. Stepney. "ChemInform Abstract: Diastereoselective Reductive Nitro-Mannich Reactions." ChemInform 43, no. 37 (August 16, 2012): no. http://dx.doi.org/10.1002/chin.201237038.
Повний текст джерелаKnappke, Christiane E. I., Sabine Grupe, Dominik Gärtner, Martin Corpet, Corinne Gosmini, and Axel Jacobi von Wangelin. "Reductive Cross-Coupling Reactions between Two Electrophiles." Chemistry - A European Journal 20, no. 23 (May 13, 2014): 6828–42. http://dx.doi.org/10.1002/chem.201402302.
Повний текст джерелаBaxter, R. M. "Reductive Dehalogenation of Environmental Contaminants: A Critical Review." Water Quality Research Journal 24, no. 2 (May 1, 1989): 299–322. http://dx.doi.org/10.2166/wqrj.1989.018.
Повний текст джерелаChitnis, Saurabh S., Alasdair P. M. Robertson, Neil Burford, Jan J. Weigand, and Roland Fischer. "Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine–antimony complexes." Chemical Science 6, no. 4 (2015): 2559–74. http://dx.doi.org/10.1039/c4sc03939d.
Повний текст джерелаRayabarapu, Dinesh Kumar, and Chien-Hong Cheng. "Novel cyclization and reductive coupling of bicyclic olefins with alkyl propiolates catalyzed by nickel complexes." Pure and Applied Chemistry 74, no. 1 (January 1, 2002): 69–75. http://dx.doi.org/10.1351/pac200274010069.
Повний текст джерелаBoll, Matthias, and Georg Fuchs. "Unusual reactions involved in anaerobic metabolism of phenolic compounds." Biological Chemistry 386, no. 10 (October 1, 2005): 989–97. http://dx.doi.org/10.1515/bc.2005.115.
Повний текст джерелаVorbeck, Claudia, Hiltrud Lenke, Peter Fischer, Jim C. Spain, and Hans-Joachim Knackmuss. "Initial Reductive Reactions in Aerobic Microbial Metabolism of 2,4,6-Trinitrotoluene." Applied and Environmental Microbiology 64, no. 1 (January 1, 1998): 246–52. http://dx.doi.org/10.1128/aem.64.1.246-252.1998.
Повний текст джерелаBacon, Mark, and W. John Ingledew. "The reductive reactions ofThiobacillus ferrooxidanson sulphur and selenium." FEMS Microbiology Letters 58, no. 2-3 (April 1989): 189–94. http://dx.doi.org/10.1111/j.1574-6968.1989.tb03042.x.
Повний текст джерелаChiu, Pauline, and Wing Chung. "Reductive Intramolecular Henry Reactions Induced by Stryker’s Reagent." Synlett 2005, no. 01 (November 29, 2004): 55–58. http://dx.doi.org/10.1055/s-2004-836044.
Повний текст джерелаMolander, Gary A., and Caryn Kenny. "Intramolecular reductive coupling reactions promoted by samarium diiodide." Journal of the American Chemical Society 111, no. 21 (October 1989): 8236–46. http://dx.doi.org/10.1021/ja00203a027.
Повний текст джерелаStuder, Armido, and Stephan Amrein. "Tin Hydride Substitutes in Reductive Radical Chain Reactions." Synthesis 2002, no. 07 (2002): 835–49. http://dx.doi.org/10.1055/s-2002-28507.
Повний текст джерелаDonohoe, Timothy J., Karl W. Ace, Paul M. Guyo, Madeleine Helliwell, and Jeffrey McKenna. "ChemInform Abstract: Reductive Aldol Reactions on Aromatic Heterocycles." ChemInform 31, no. 18 (June 8, 2010): no. http://dx.doi.org/10.1002/chin.200018084.
Повний текст джерелаFürstner, Alois. "Synthesis and Reductive Elimination Reactions of Aryl Thioglycosides." Liebigs Annalen der Chemie 1993, no. 11 (November 12, 1993): 1211–17. http://dx.doi.org/10.1002/jlac.1993199301196.
Повний текст джерелаStreuff, Jan. "Reductive Umpolung Reactions with Low-Valent Titanium Catalysts." Chemical Record 14, no. 6 (September 19, 2014): 1100–1113. http://dx.doi.org/10.1002/tcr.201402058.
Повний текст джерелаCzaplik, Waldemar M., Matthias Mayer, and Axel Jacobi von Wangelin. "Iron-Catalyzed Reductive Aryl-Alkenyl Cross-Coupling Reactions." ChemCatChem 3, no. 1 (September 23, 2010): 135–38. http://dx.doi.org/10.1002/cctc.201000276.
Повний текст джерелаBack, Thomas G. "ChemInform Abstract: Free-Radical Reactions and Reductive Deselenations." ChemInform 31, no. 32 (June 3, 2010): no. http://dx.doi.org/10.1002/chin.200032234.
Повний текст джерелаReichard, Holly A., Martin McLaughlin, Ming Z. Chen, and Glenn C. Micalizio. "Regioselective Reductive Cross-Coupling Reactions of Unsymmetrical Alkynes." European Journal of Organic Chemistry 2010, no. 3 (January 2010): 391–409. http://dx.doi.org/10.1002/ejoc.200901094.
Повний текст джерелаBoll, Matthias, Oliver Einsle, Ulrich Ermler, Peter M. H. Kroneck, and G. Matthias Ullmann. "Structure and Function of the Unusual Tungsten Enzymes Acetylene Hydratase and Class II Benzoyl-Coenzyme A Reductase." Journal of Molecular Microbiology and Biotechnology 26, no. 1-3 (2016): 119–37. http://dx.doi.org/10.1159/000440805.
Повний текст джерелаLin, Chia-Hsin, Bor-Cherng Hong, and Gene-Hsiang Lee. "Asymmetric synthesis of functionalized pyrrolizidines by an organocatalytic and pot-economy strategy." RSC Advances 6, no. 10 (2016): 8243–47. http://dx.doi.org/10.1039/c5ra25103f.
Повний текст джерелаKisała, Joanna, Bogdan Stefan Vasile, Anton Ficai, Denisa Ficai, Renata Wojnarowska-Nowak, and Tomasz Szreder. "Reductive Photodegradation of 4,4′-Isopropylidenebis(2,6-dibromophenol) on Fe3O4 Surface." Materials 16, no. 12 (June 14, 2023): 4380. http://dx.doi.org/10.3390/ma16124380.
Повний текст джерелаSalem, Mohammed A., Moustafa A. Gouda, and Ghada G. El-Bana. "Chemistry of 2-(Piperazin-1-yl) Quinoline-3-Carbaldehydes." Mini-Reviews in Organic Chemistry 19, no. 4 (June 2022): 480–95. http://dx.doi.org/10.2174/1570193x18666211001124510.
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