Статті в журналах з теми "Coupling methodologies"
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Brandmeyer, Jo Ellen, and Hassan A. Karimi. "Coupling methodologies for environmental models." Environmental Modelling & Software 15, no. 5 (July 2000): 479–88. http://dx.doi.org/10.1016/s1364-8152(00)00027-x.
Повний текст джерелаTollit, Brendan, Alan Charles, William Poole, Andrew Cox, Glynn Hosking, Ben Lindley, Peter Smith, Andy Smethurst, and Jean Lavarenne. "WHOLE CORE COUPLING METHODOLOGIES WITHIN WIMS." EPJ Web of Conferences 247 (2021): 06006. http://dx.doi.org/10.1051/epjconf/202124706006.
Повний текст джерелаRibas, Xavi, and Imma Güell. "Cu(I)/Cu(III) catalytic cycle involved in Ullmann-type cross-coupling reactions." Pure and Applied Chemistry 86, no. 3 (March 20, 2014): 345–60. http://dx.doi.org/10.1515/pac-2013-1104.
Повний текст джерелаFarhi, Jonathan, Ioannis N. Lykakis, and George E. Kostakis. "Metal-Catalysed A3 Coupling Methodologies: Classification and Visualisation." Catalysts 12, no. 6 (June 15, 2022): 660. http://dx.doi.org/10.3390/catal12060660.
Повний текст джерелаHubbard, Amber M., Yixin Ren, Dominik Konkolewicz, Alireza Sarvestani, Catalin R. Picu, Gary S. Kedziora, Ajit Roy, Vikas Varshney, and Dhriti Nepal. "Vitrimer Transition Temperature Identification: Coupling Various Thermomechanical Methodologies." ACS Applied Polymer Materials 3, no. 4 (March 4, 2021): 1756–66. http://dx.doi.org/10.1021/acsapm.0c01290.
Повний текст джерелаTerra, Bruna S., and Fernando Macedo. "Progress in the intermolecular pinacol cross coupling methodologies." Arkivoc 2012, no. 1 (December 11, 2011): 134–51. http://dx.doi.org/10.3998/ark.5550190.0013.104.
Повний текст джерелаHof, Fraser, Michael Schär, Denise M Scofield, Felix Fischer, François Diederich, and Sergey Sergeyev. "Preparation ofTröger Base Derivatives by Cross-Coupling Methodologies." Helvetica Chimica Acta 88, no. 8 (August 2005): 2333–44. http://dx.doi.org/10.1002/hlca.200590168.
Повний текст джерелаTerra, Bruna S., and Jr Macedo Fernando. "ChemInform Abstract: Progress in Intermolecular Pinacol Cross-Coupling Methodologies." ChemInform 43, no. 16 (March 22, 2012): no. http://dx.doi.org/10.1002/chin.201216251.
Повний текст джерелаMiyake, Garret, Bin Liu, and Chern-Hooi Lim. "Transition-Metal-Free, Visible-Light-Promoted C–S Cross-Coupling through Intermolecular Charge Transfer." Synlett 29, no. 19 (August 8, 2018): 2449–55. http://dx.doi.org/10.1055/s-0037-1610230.
Повний текст джерелаAndrade, Marta A., and Luísa M. D. R. S. Martins. "New Trends in C–C Cross-Coupling Reactions: The Use of Unconventional Conditions." Molecules 25, no. 23 (November 24, 2020): 5506. http://dx.doi.org/10.3390/molecules25235506.
Повний текст джерелаBagdi, Avik Kumar, Matiur Rahman, Dhananjay Bhattacherjee, Grigory V. Zyryanov, Sumit Ghosh, Oleg N. Chupakhin, and Alakananda Hajra. "Visible light promoted cross-dehydrogenative coupling: a decade update." Green Chemistry 22, no. 20 (2020): 6632–81. http://dx.doi.org/10.1039/d0gc02437f.
Повний текст джерелаHu, Fangdong, Ying Xia, Chen Ma, Yan Zhang, and Jianbo Wang. "C–H bond functionalization based on metal carbene migratory insertion." Chemical Communications 51, no. 38 (2015): 7986–95. http://dx.doi.org/10.1039/c5cc00497g.
Повний текст джерелаPatel, Heta A., Viraj J. Bhanvadia, Hemant M. Mande, Sanjio S. Zade, and Arun L. Patel. "Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling." Organic & Biomolecular Chemistry 17, no. 43 (2019): 9467–78. http://dx.doi.org/10.1039/c9ob01762c.
Повний текст джерелаCardini, Andrea. "Methodologies to Measure the CP Structure of the Higgs Yukawa Coupling to Tau Leptons." Universe 8, no. 5 (April 21, 2022): 256. http://dx.doi.org/10.3390/universe8050256.
Повний текст джерелаRonson, Thomas O., Martin H. H. Voelkel, Richard J. K. Taylor, and Ian J. S. Fairlamb. "Macrocyclic polyenynes: a stereoselective route to vinyl-ether-containing skipped diene systems." Chemical Communications 51, no. 38 (2015): 8034–36. http://dx.doi.org/10.1039/c5cc02091c.
Повний текст джерелаLüdtke, Niklas, Nikos K. Logothetis, and Stefano Panzeri. "Testing methodologies for the nonlinear analysis of causal relationships in neurovascular coupling." Magnetic Resonance Imaging 28, no. 8 (October 2010): 1113–19. http://dx.doi.org/10.1016/j.mri.2010.03.028.
Повний текст джерелаKostas, Ioannis D. "Editorial Catalysts: Special Issue on Transition Metal Catalyzed Cross-Coupling Reactions." Catalysts 11, no. 4 (April 7, 2021): 473. http://dx.doi.org/10.3390/catal11040473.
Повний текст джерелаRifhat Bibi, Rifhat Bibi, Muhammad Yaseen Muhammad Yaseen, Haseen Ahmad Haseen Ahmad, Ismat Ullah Khan Ismat Ullah Khan, Shaista Parveen Shaista Parveen, and Abbas Hassan Abbas Hassan. "Palladium Catalyzed Synthesis of Phenylquinoxaline-Alkyne Derivatives via Sonogashira Cross Coupling Reaction." Journal of the chemical society of pakistan 43, no. 1 (2021): 95. http://dx.doi.org/10.52568/000550.
Повний текст джерелаRifhat Bibi, Rifhat Bibi, Muhammad Yaseen Muhammad Yaseen, Haseen Ahmad Haseen Ahmad, Ismat Ullah Khan Ismat Ullah Khan, Shaista Parveen Shaista Parveen, and Abbas Hassan Abbas Hassan. "Palladium Catalyzed Synthesis of Phenylquinoxaline-Alkyne Derivatives via Sonogashira Cross Coupling Reaction." Journal of the chemical society of pakistan 43, no. 1 (2021): 95. http://dx.doi.org/10.52568/000550/jcsp/43.01.2021.
Повний текст джерелаRifhat Bibi, Rifhat Bibi, Muhammad Yaseen Muhammad Yaseen, Haseen Ahmad Haseen Ahmad, Ismat Ullah Khan Ismat Ullah Khan, Shaista Parveen Shaista Parveen, and Abbas Hassan Abbas Hassan. "Palladium Catalyzed Synthesis of Phenylquinoxaline-Alkyne Derivatives via Sonogashira Cross Coupling Reaction." Journal of the chemical society of pakistan 43, no. 1 (2021): 95. http://dx.doi.org/10.52568/000009.
Повний текст джерелаSoural, Miroslav, and Veronika Ručilová. "Recent Advances in the Applications of Triethylsilane in Organic Synthesis." Synthesis 50, no. 19 (July 2, 2018): 3809–24. http://dx.doi.org/10.1055/s-0037-1610107.
Повний текст джерелаJessen, Henning J., Nisar Ahmed, and Alexandre Hofer. "Phosphate esters and anhydrides – recent strategies targeting nature's favoured modifications." Org. Biomol. Chem. 12, no. 22 (2014): 3526–30. http://dx.doi.org/10.1039/c4ob00478g.
Повний текст джерелаGhosh, Anogh, Pranjal Pyne, Sumit Ghosh, Debashis Ghosh, Souvik Majumder, and Alakananda Hajra. "Visible-light-induced metal-free coupling of C(sp3)–H sources with heteroarenes." Green Chemistry 24, no. 8 (2022): 3056–80. http://dx.doi.org/10.1039/d1gc04384f.
Повний текст джерелаTeng, Yun Chao, Zhen Chao Teng, Yu Liu, Xiao Yan Liu, Ya Dong Zhou, Jia Lin Liu, and Bo Li. "A Review of the Research on Thermo-Hydro-Mechanical Coupling for the Frozen Soil." Geofluids 2022 (March 21, 2022): 1–11. http://dx.doi.org/10.1155/2022/8274137.
Повний текст джерелаStrauss, Christopher R. "Invited Review. A Combinatorial Approach to the Development of Environmentally Benign Organic Chemical Preparations." Australian Journal of Chemistry 52, no. 2 (1999): 83. http://dx.doi.org/10.1071/c98156.
Повний текст джерелаVeitl, A., T. Gordon, A. Van De Sand, M. Howell, M. Valasek, O. Vaculin, and P. Steinbauer. "Methodologies for Coupling Simulation Models and Codes in Mechatronic System Analysis and Design." Vehicle System Dynamics 33, sup1 (January 1, 1999): 231–43. http://dx.doi.org/10.1080/00423114.1999.12063084.
Повний текст джерелаSantos, A., Ana Mortinho, and M. Marques. "Metal-Catalyzed Cross-Coupling Reactions on Azaindole Synthesis and Functionalization." Molecules 23, no. 10 (October 17, 2018): 2673. http://dx.doi.org/10.3390/molecules23102673.
Повний текст джерелаChen, Qing-An, Wei-Song Zhang, and Yan-Cheng Hu. "Isoprene: A Promising Coupling Partner in C–H Functionalizations." Synlett 31, no. 17 (July 2, 2020): 1649–55. http://dx.doi.org/10.1055/s-0040-1707172.
Повний текст джерелаSoares, Delfim. "Coupled Numerical Methods to Analyze Interacting Acoustic-Dynamic Models by Multidomain Decomposition Techniques." Mathematical Problems in Engineering 2011 (2011): 1–28. http://dx.doi.org/10.1155/2011/245170.
Повний текст джерелаSobrinho, João, Hilda de Pablo, Francisco Campuzano, and Ramiro Neves. "Coupling Rivers and Estuaries with an Ocean Model: An Improved Methodology." Water 13, no. 16 (August 21, 2021): 2284. http://dx.doi.org/10.3390/w13162284.
Повний текст джерелаLinars, Artis, Ivars Silamikelis, Dita Gudra, Ance Roga, and Davids Fridmanis. "OverFlap PCR: A reliable approach for generating plasmid DNA libraries containing random sequences without a template bias." PLOS ONE 17, no. 8 (August 8, 2022): e0262968. http://dx.doi.org/10.1371/journal.pone.0262968.
Повний текст джерелаPich, Antonio, та Antonio Rodríguez-Sánchez. "Updated determination of αs(mτ2) from τ decays". Modern Physics Letters A 31, № 30 (15 вересня 2016): 1630032. http://dx.doi.org/10.1142/s0217732316300329.
Повний текст джерелаHusson, Jérôme, and Michael Knorr. "Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines." Beilstein Journal of Organic Chemistry 8 (March 12, 2012): 379–89. http://dx.doi.org/10.3762/bjoc.8.41.
Повний текст джерелаShaya, Janah, Gabriel Correia, Benoît Heinrich, Jean-Charles Ribierre, Kyriaki Polychronopoulou, Loïc Mager, and Stéphane Méry. "Functionalization of Biphenylcarbazole (CBP) with Siloxane-Hybrid Chains for Solvent-Free Liquid Materials." Molecules 27, no. 1 (December 24, 2021): 89. http://dx.doi.org/10.3390/molecules27010089.
Повний текст джерелаZhao, Baoping, and Victor Snieckus. "Integrated aromatic metalation - cross coupling methodologies. A concise synthesis of the azafluoranthene alkaloid imeluteine." Tetrahedron Letters 32, no. 39 (September 1991): 5277–78. http://dx.doi.org/10.1016/s0040-4039(00)92363-3.
Повний текст джерелаYousaf, Muhammad, Ameer Fawad Zahoor, Rabia Akhtar, Matloob Ahmad, and Shazia Naheed. "Development of green methodologies for Heck, Chan–Lam, Stille and Suzuki cross-coupling reactions." Molecular Diversity 24, no. 3 (August 28, 2019): 821–39. http://dx.doi.org/10.1007/s11030-019-09988-7.
Повний текст джерелаLeysen, Pieter, Silvia Quattrosoldi, Elisabetta Salatelli, and Guy Koeckelberghs. "Investigation of the dithieno[3,2-b:2′,3′-d]pyrrole polymerization using cross-coupling and cationic mechanisms." Polymer Chemistry 10, no. 8 (2019): 1010–17. http://dx.doi.org/10.1039/c8py01176a.
Повний текст джерелаVerrier, Cécile, Pierrik Lassalas, Laure Théveau, Guy Quéguiner, François Trécourt, Francis Marsais, and Christophe Hoarau. "Recent advances in direct C–H arylation: Methodology, selectivity and mechanism in oxazole series." Beilstein Journal of Organic Chemistry 7 (November 29, 2011): 1584–601. http://dx.doi.org/10.3762/bjoc.7.187.
Повний текст джерелаOdell, Luke, Mats Larhed, and Linda Åkerbladh. "Palladium-Catalyzed Molybdenum Hexacarbonyl-Mediated Gas-Free Carbonylative Reactions." Synlett 30, no. 02 (October 2, 2018): 141–55. http://dx.doi.org/10.1055/s-0037-1610294.
Повний текст джерелаJoshi, Alok, and Won-jong Kim. "Modeling and Multivariable Control Design Methodologies for Hexapod-Based Satellite Vibration Isolation." Journal of Dynamic Systems, Measurement, and Control 127, no. 4 (November 30, 2004): 700–704. http://dx.doi.org/10.1115/1.2101842.
Повний текст джерелаMasouman, Ashkan, and Charles Harvie. "Forecasting, impact analysis and uncertainty propagation in regional integrated models: A case study of Australia." Environment and Planning B: Urban Analytics and City Science 47, no. 1 (April 16, 2018): 65–83. http://dx.doi.org/10.1177/2399808318767128.
Повний текст джерелаYu, Hui, та Feng Xu. "Non-noble metal-catalyzed cross-dehydrogenation coupling (CDC) involving ether α-C(sp3)–H to construct C–C bonds". Beilstein Journal of Organic Chemistry 19 (6 вересня 2023): 1259–88. http://dx.doi.org/10.3762/bjoc.19.94.
Повний текст джерелаBrevault, Loïc, Mathieu Balesdent, and Sébastien Defoort. "Preliminary study on launch vehicle design: Applications of multidisciplinary design optimization methodologies." Concurrent Engineering 26, no. 1 (November 6, 2017): 93–103. http://dx.doi.org/10.1177/1063293x17737131.
Повний текст джерелаGuzmán, M. Orozco, S. Obredor Castro, F. Mejía Acuña, and E. Silvera Malo. "Importance of coupling the teaching methodologies of mathematics with the learning styles of digital natives." Journal of Physics: Conference Series 1414 (November 2019): 012004. http://dx.doi.org/10.1088/1742-6596/1414/1/012004.
Повний текст джерелаAsadizadeh, Mostafa, Hossein Masoumi, Hamid Roshan, and Ahmadreza Hedayat. "Coupling Taguchi and Response Surface Methodologies for the Efficient Characterization of Jointed Rocks’ Mechanical Properties." Rock Mechanics and Rock Engineering 52, no. 11 (May 25, 2019): 4807–19. http://dx.doi.org/10.1007/s00603-019-01853-1.
Повний текст джерелаClewell III, Harvey J. "Coupling of computer modeling with in vitro methodologies to reduce animal usage in toxicity testing." Toxicology Letters 68, no. 1-2 (May 1993): 101–17. http://dx.doi.org/10.1016/0378-4274(93)90123-f.
Повний текст джерелаDorn, Viviana, Emilio Lorenzo Martínez, and Gabriel Radivoy. "Applications of Computational and NMR Methodologies to the Study of Homoallylic Alcohols Diastereomers." Proceedings 9, no. 1 (November 14, 2018): 12. http://dx.doi.org/10.3390/ecsoc-22-05782.
Повний текст джерелаKairytė, Agnė, Saulius Vaitkus, and Sigitas Vėjelis. "Titanate-Based Surface Modification of Paper Waste Particles and its Impact on Rigid Polyurethane Foam Properties." Key Engineering Materials 721 (December 2016): 58–62. http://dx.doi.org/10.4028/www.scientific.net/kem.721.58.
Повний текст джерелаEjjoummany, Abdelaziz, Rabia Belaroussi, Ahmed El Hakmaoui, Mohamed Akssira, Gérald Guillaumet, Frédéric Buron, and Sylvain Routier. "Regioselective Synthesis of New 2,4-(Het)aryl-3H-pyrido[1′,2′:1,5]pyrazolo[4,3-d]pyrimidines Involving Palladium-Catalyzed Cross-Coupling Reactions." Molecules 23, no. 11 (October 23, 2018): 2740. http://dx.doi.org/10.3390/molecules23112740.
Повний текст джерелаFañanás-Mastral, Martín, Eva Rivera-Chao, and Laura Fra. "Synergistic Bimetallic Catalysis for Carboboration of Unsaturated Hydrocarbons." Synthesis 50, no. 19 (July 9, 2018): 3825–32. http://dx.doi.org/10.1055/s-0037-1610434.
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