Статті в журналах з теми "C-N bond forming processes"
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Valdés, Carlos, Raquel Barroso, and María Cabal. "Pd-catalyzed Auto-Tandem Cascades Based on N-Sulfonylhydrazones: Hetero- and Carbocyclization Processes." Synthesis 28, no. 19 (August 10, 2017): 4434–47. http://dx.doi.org/10.1055/s-0036-1588535.
Повний текст джерелаBuchspies, Jonathan, Md Mahbubur Rahman, and Michal Szostak. "Transamidation of Amides and Amidation of Esters by Selective N–C(O)/O–C(O) Cleavage Mediated by Air- and Moisture-Stable Half-Sandwich Nickel(II)–NHC Complexes." Molecules 26, no. 1 (January 2, 2021): 188. http://dx.doi.org/10.3390/molecules26010188.
Повний текст джерелаCorrea, Arkaitz, та Marcos Segundo. "Cross-Dehydrogenative Coupling Reactions for the Functionalization of α-Amino Acid Derivatives and Peptides". Synthesis 50, № 15 (25 червня 2018): 2853–66. http://dx.doi.org/10.1055/s-0037-1610073.
Повний текст джерелаYoun, So Won. "Transition-Metal-Catalyzed Annulative Coupling Cascade for the Synthesis of 3-Methyleneisoindolin-1-ones." Synthesis 52, no. 06 (January 15, 2020): 807–18. http://dx.doi.org/10.1055/s-0039-1690046.
Повний текст джерелаMartín, Cristina del Mar García, José Ignacio Hernández García, Sebastián Bonardd, and David Díaz Díaz. "Lignin-Based Catalysts for C–C Bond-Forming Reactions." Molecules 28, no. 8 (April 16, 2023): 3513. http://dx.doi.org/10.3390/molecules28083513.
Повний текст джерелаMcNally, Andrew, Ryan Dolewski, and Michael Hilton. "4-Selective Pyridine Functionalization Reactions via Heterocyclic Phosphonium Salts." Synlett 29, no. 01 (December 12, 2017): 08–14. http://dx.doi.org/10.1055/s-0036-1591850.
Повний текст джерелаDaoust, Benoit, Nicolas Gilbert, Paméla Casault, François Ladouceur, and Simon Ricard. "1,2-Dihaloalkenes in Metal-Catalyzed Reactions." Synthesis 50, no. 16 (July 9, 2018): 3087–113. http://dx.doi.org/10.1055/s-0037-1610174.
Повний текст джерелаTodd, David P., Benjamin B. Thompson, Alex J. Nett, and John Montgomery. "Deoxygenative C–C Bond-Forming Processes via a Net Four-Electron Reductive Coupling." Journal of the American Chemical Society 137, no. 40 (October 5, 2015): 12788–91. http://dx.doi.org/10.1021/jacs.5b08448.
Повний текст джерелаLiu, Jialin, Xiaoyu Xiong, Jie Chen, Yuntao Wang, Ranran Zhu, and Jianhui Huang. "Double C–H Activation for the C–C bond Formation Reactions." Current Organic Synthesis 15, no. 7 (October 16, 2018): 882–903. http://dx.doi.org/10.2174/1570179415666180720111422.
Повний текст джерелаTodd, David P., Benjamin B. Thompson, Alex J. Nett, and John Montgomery. "ChemInform Abstract: Deoxygenative C-C Bond-Forming Processes via a Net Four-Electron Reductive Coupling." ChemInform 47, no. 12 (March 2016): no. http://dx.doi.org/10.1002/chin.201612061.
Повний текст джерелаGray, Vincent James, and Jonathan D. Wilden. "The chemistry of ynol and thioynol ethers." Organic & Biomolecular Chemistry 14, no. 41 (2016): 9695–711. http://dx.doi.org/10.1039/c6ob01776b.
Повний текст джерелаBuzzetti, Luca, Alexis Prieto, Sudipta Raha Roy, and Paolo Melchiorre. "Radical-Based C−C Bond-Forming Processes Enabled by the Photoexcitation of 4-Alkyl-1,4-dihydropyridines." Angewandte Chemie 129, no. 47 (October 24, 2017): 15235–39. http://dx.doi.org/10.1002/ange.201709571.
Повний текст джерелаBuzzetti, Luca, Alexis Prieto, Sudipta Raha Roy, and Paolo Melchiorre. "Radical-Based C−C Bond-Forming Processes Enabled by the Photoexcitation of 4-Alkyl-1,4-dihydropyridines." Angewandte Chemie International Edition 56, no. 47 (October 24, 2017): 15039–43. http://dx.doi.org/10.1002/anie.201709571.
Повний текст джерелаChiummiento, Lucia, Rosarita D’Orsi, Maria Funicello, and Paolo Lupattelli. "Last Decade of Unconventional Methodologies for the Synthesis of Substituted Benzofurans." Molecules 25, no. 10 (May 16, 2020): 2327. http://dx.doi.org/10.3390/molecules25102327.
Повний текст джерелаHigham, Joe I., and James A. Bull. "Transient imine directing groups for the C–H functionalisation of aldehydes, ketones and amines: an update 2018–2020." Organic & Biomolecular Chemistry 18, no. 37 (2020): 7291–315. http://dx.doi.org/10.1039/d0ob01587c.
Повний текст джерелаNie, Siyuan, Wei Shen, Shengnan Shen, Hui Li, Yuanhui Pan, Yuechang Sun, Yinghua Chen, and Haiqin Qi. "Effects of Vacancy and Hydrogen on the Growth and Morphology of N-Type Phosphorus-Doped Diamond Surfaces." Applied Sciences 11, no. 4 (February 22, 2021): 1896. http://dx.doi.org/10.3390/app11041896.
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 джерелаHuang, Xiaohua, Kevin W. Anderson, Danilo Zim, Lei Jiang, Artis Klapars, and Stephen L. Buchwald. "Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions." Journal of the American Chemical Society 125, no. 22 (June 2003): 6653–55. http://dx.doi.org/10.1021/ja035483w.
Повний текст джерелаVinogradova, Ekaterina V. "Organometallic chemical biology: an organometallic approach to bioconjugation." Pure and Applied Chemistry 89, no. 11 (October 26, 2017): 1619–40. http://dx.doi.org/10.1515/pac-2017-0207.
Повний текст джерелаMartínez-García, Lucas, Rubén Lobato, Gustavo Prado, Pablo Monje, F. Javier Sardina, and M. Rita Paleo. "C–C Bond-Forming and Bond-Breaking Processes from the Reaction of Diesters with Me3SnLi. Synthesis of Complex Bridged Polycycles and Dialkyl Aromatic Compounds." Journal of Organic Chemistry 84, no. 4 (January 21, 2019): 1887–97. http://dx.doi.org/10.1021/acs.joc.8b02891.
Повний текст джерелаLI, Y., and T. J. MARKS. "ChemInform Abstract: Organolanthanoid-Catalyzed Intra- and Intermolecular Tandem C-N and C-C Bond-Forming Processes of Aminodialkenes, Aminodialkynes, Aminoalkeneynes, and Aminoalkynes. New Regiospecific Approaches to Pyrrolizidine, Indolizidine, Pyrrole,." ChemInform 29, no. 27 (June 21, 2010): no. http://dx.doi.org/10.1002/chin.199827135.
Повний текст джерелаSuárez-Pantiga, Samuel, and José M. González. "Electrophilic activation of unsaturated systems: Applications to selective organic synthesis." Pure and Applied Chemistry 85, no. 4 (March 13, 2013): 721–39. http://dx.doi.org/10.1351/pac-con-12-10-24.
Повний текст джерелаKamanna, Kantharaju, and Santosh Y. Khatavi. "Microwave-accelerated Carbon-carbon and Carbon-heteroatom Bond Formation via Multi-component Reactions: A Brief Overview." Current Microwave Chemistry 7, no. 1 (June 23, 2020): 23–39. http://dx.doi.org/10.2174/2213346107666200218124147.
Повний текст джерелаLi, Yanwu, and Tobin J. Marks. "Organolanthanide-Catalyzed Intra- and Intermolecular Tandem C−N and C−C Bond-Forming Processes of Aminodialkenes, Aminodialkynes, Aminoalkeneynes, and Aminoalkynes. New Regiospecific Approaches to Pyrrolizidine, Indolizidine, Pyrrole, and Pyrazine Skeletons." Journal of the American Chemical Society 120, no. 8 (March 1998): 1757–71. http://dx.doi.org/10.1021/ja972643t.
Повний текст джерелаYeagley, Andrew A., Melissa A. Lowder, and Jason J. Chruma. "Tandem C−C Bond-Forming Processes: Interception of the Pd-Catalyzed Decarboxylative Allylation of Allyl Diphenylglycinate Imines with Activated Olefins." Organic Letters 11, no. 17 (September 3, 2009): 4022–25. http://dx.doi.org/10.1021/ol901745x.
Повний текст джерелаLi, Ningbo, Qi Fan, Li Xu, Rong Ma, Shitang Xu, Jie Qiao, Xinhua Xu, Rui Guo, and Kemin Yun. "Air-stable Organoantimony (III) Perfluoroalkyl(aryl)sulfonate complexes as highly efficient, selective, and recyclable catalysts for C–C and C–N bond-forming reactions." Molecular Catalysis 511 (July 2021): 111727. http://dx.doi.org/10.1016/j.mcat.2021.111727.
Повний текст джерелаWang, Yuefei, Kunji Chen, Xinye Qian, Zhonghui Fang, Wei Li, and Jun Xu. "The role of biasing electric field in intrinsic resistive switching characteristics of highly silicon-rich a-SiOx films." Canadian Journal of Physics 92, no. 7/8 (July 2014): 589–92. http://dx.doi.org/10.1139/cjp-2013-0569.
Повний текст джерелаGaona, Aidé, Urbano Díaz, and Avelino Corma. "Functional Acid and Base Hybrid Catalysts Organized by Associated (Organo)aluminosilicate Layers for C–C Bond Forming Reactions and Tandem Processes." Chemistry of Materials 29, no. 4 (February 14, 2017): 1599–612. http://dx.doi.org/10.1021/acs.chemmater.6b04563.
Повний текст джерелаPopov, Stasik, Brian Shao, Alex L. Bagdasarian, Tyler R. Benton, Luyi Zou, Zhongyue Yang, K. N. Houk, and Hosea M. Nelson. "Teaching an old carbocation new tricks: Intermolecular C–H insertion reactions of vinyl cations." Science 361, no. 6400 (July 26, 2018): 381–87. http://dx.doi.org/10.1126/science.aat5440.
Повний текст джерелаGuerra, Walter D., María E. Budén, Silvia M. Barolo, Roberto A. Rossi, and Adriana B. Pierini. "Intra- vs inter-molecular electron transfer processes in C N bond forming reactions. Photochemical, photophysical and theoretical study of 2′-halo-[1,1′-biphenyl]-2-amines." Tetrahedron 72, no. 48 (December 2016): 7796–804. http://dx.doi.org/10.1016/j.tet.2016.08.051.
Повний текст джерелаLopat’eva, Elena R., Igor B. Krylov, Dmitry A. Lapshin, and Alexander O. Terent’ev. "Redox-active molecules as organocatalysts for selective oxidative transformations – an unperceived organocatalysis field." Beilstein Journal of Organic Chemistry 18 (December 9, 2022): 1672–95. http://dx.doi.org/10.3762/bjoc.18.179.
Повний текст джерелаCera, Gianpiero, Michel Chiarucci, and Marco Bandini. "Accessing chemical diversity by stereoselective gold-catalyzed manipulation of allylic and propargylic alcohols." Pure and Applied Chemistry 84, no. 8 (February 3, 2012): 1673–84. http://dx.doi.org/10.1351/pac-con-11-09-05.
Повний текст джерелаCrochet, Pascale, and Victorio Cadierno. "Arene-Osmium(II) Complexes in Homogeneous Catalysis." Inorganics 9, no. 7 (July 12, 2021): 55. http://dx.doi.org/10.3390/inorganics9070055.
Повний текст джерелаSoengas, Raquel G., and Humberto Rodríguez-Solla. "Modern Synthetic Methods for the Stereoselective Construction of 1,3-Dienes." Molecules 26, no. 2 (January 6, 2021): 249. http://dx.doi.org/10.3390/molecules26020249.
Повний текст джерелаProtti, Stefano, Daniele Dondi, Maurizio Fagnoni, and Angelo Albini. "Photochemistry in synthesis: Where, when, and why." Pure and Applied Chemistry 79, no. 11 (January 1, 2007): 1929–38. http://dx.doi.org/10.1351/pac200779111929.
Повний текст джерелаLuong, Truc Thanh, Reyhaneh Tirgar, Melissa E. Reardon-Robinson, Andrzej Joachimiak, Jerzy Osipiuk, and Hung Ton-That. "Structural Basis of a Thiol-Disulfide Oxidoreductase in the Hedgehog-Forming ActinobacteriumCorynebacterium matruchotii." Journal of Bacteriology 200, no. 9 (February 12, 2018): e00783-17. http://dx.doi.org/10.1128/jb.00783-17.
Повний текст джерелаYamada, Tsuyoshi, Jing Jiang, Naoya Ito, Kwihwan Park, Hayato Masuda, Chikara Furugen, Moeka Ishida, Seiya Ōtori, and Hironao Sajiki. "Development of Facile and Simple Processes for the Heterogeneous Pd-Catalyzed Ligand-Free Continuous-Flow Suzuki–Miyaura Coupling." Catalysts 10, no. 10 (October 19, 2020): 1209. http://dx.doi.org/10.3390/catal10101209.
Повний текст джерелаDominguez, Beatriz, Beatriz Iglesias, and Angel R. de Lera. "ChemInform Abstract: A Comprehensive Survey of Stille-Type C(sp2)-C(sp2) Single Bond Forming Processes in the Synthesis of Retinoic Acid and Analogues." ChemInform 31, no. 12 (June 9, 2010): no. http://dx.doi.org/10.1002/chin.200012272.
Повний текст джерелаMeng, Qingyan, Syed G. A. Moinuddin, Sung-Jin Kim, Diana L. Bedgar, Michael A. Costa, Dennis G. Thomas, Robert P. Young, et al. "Pterocarpan synthase (PTS) structures suggest a common quinone methide–stabilizing function in dirigent proteins and proteins with dirigent-like domains." Journal of Biological Chemistry 295, no. 33 (June 21, 2020): 11584–601. http://dx.doi.org/10.1074/jbc.ra120.012444.
Повний текст джерелаByrne, Paul G., M. Esther Garcia, John C. Jeffery, Paul Sherwood, and F. Gordon A. Stone. "Reactions between µ-alkylidyne iron–molybdenum complexes and but-2-yne: unusually facile C–C bond forming processes accompanied by hydrogen migration between carbon centres." J. Chem. Soc., Chem. Commun., no. 2 (1987): 53–55. http://dx.doi.org/10.1039/c39870000053.
Повний текст джерелаHuang, Xiaohua, Kevin W. Anderson, Danilo Zim, Lei Jiang, Artis Klapars, and Stephen L. Buchwald. "Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions [J. Am. Chem. Soc.2003,125, 6653−6655]." Journal of the American Chemical Society 125, no. 35 (September 2003): 10767. http://dx.doi.org/10.1021/ja033450a.
Повний текст джерелаStepanenko, D. O., O. M. Grishin, and A. I. Belkova. "Analitical and experimental studies of properties of slag and slag-forming mixtures of steelmaking production." Fundamental and applied problems of ferrous metallurgy 37 (2023): 260–70. http://dx.doi.org/10.52150/2522-9117-2023-37-260-270.
Повний текст джерелаTetteh, Samuel. "A Computational and Structural Database Study of the Metal-Carbene Bond in Groups IA, IIA, and IIIA Imidazol-2-Ylidene Complexes." Journal of Chemistry 2019 (December 24, 2019): 1–9. http://dx.doi.org/10.1155/2019/5675870.
Повний текст джерелаTeichert, Johannes F., and Lea T. Brechmann. "Catch It If You Can: Copper-Catalyzed (Transfer) Hydrogenation Reactions and Coupling Reactions by Intercepting Reactive Intermediates Thereof." Synthesis 52, no. 17 (July 13, 2020): 2483–96. http://dx.doi.org/10.1055/s-0040-1707185.
Повний текст джерелаHölscher, Markus, Christoph Gürtler, Wilhelm Keim, Thomas E. Müller, Martina Peters, and Walter Leitner. "Carbon Dioxide as a Carbon Resource – Recent Trends and Perspectives." Zeitschrift für Naturforschung B 67, no. 10 (October 1, 2012): 961–75. http://dx.doi.org/10.5560/znb.2012-0219.
Повний текст джерелаZhou, Ru Jin, Min Huang, and Song Shan Qiu. "Study of Interior Wall Coating Based on Metakaolinand Modified Starch." Advanced Materials Research 239-242 (May 2011): 1030–35. http://dx.doi.org/10.4028/www.scientific.net/amr.239-242.1030.
Повний текст джерелаWang, Shuai, Iker Agirrezabal-Telleria, Aditya Bhan, Dante Simonetti, Kazuhiro Takanabe, and Enrique Iglesia. "Catalytic routes to fuels from C1 and oxygenate molecules." Faraday Discussions 197 (2017): 9–39. http://dx.doi.org/10.1039/c7fd00018a.
Повний текст джерелаKochetova, Ludmila B., and Tatiana P. Kustova. "Kinetics and mechanism of acyl transfer reactions. Part 16. Quantum chemical simulation of mechanism of N-methylaniline sulfonation in aqueous 1,4-dioxane." Butlerov Communications 61, no. 1 (January 31, 2020): 1–8. http://dx.doi.org/10.37952/roi-jbc-01/20-61-1-1.
Повний текст джерелаSun, Chang Q. "Origin and Processes of O-Cu(001) and the O-Cu(110) Biphase Ordering." International Journal of Modern Physics B 12, no. 09 (April 10, 1998): 951–64. http://dx.doi.org/10.1142/s0217979298000533.
Повний текст джерелаDELGADO, G. E., Asiloé J. MORA, T. GONZÁLEZ, I. SANTOS, P. RIVAS, and L. E. SEIJAS. "SOLVENT-FREE SYNTHESIS AND CRYSTAL STRUCTURE OF rac-2-THIOHYDANTOIN-VALINE." Periódico Tchê Química 16, no. 31 (January 20, 2019): 347–52. http://dx.doi.org/10.52571/ptq.v16.n31.2019.353_periodico31_pgs_347_352.pdf.
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