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Artykuły w czasopismach na temat "Carbon-Nitrozen bond(C-N) formation"
Cataldo, Franco. "Cyanopolyynes: carbon chains formation in a carbon arc mimicking the formation of carbon chains in the circumstellar medium". International Journal of Astrobiology 3, nr 3 (lipiec 2004): 237–46. http://dx.doi.org/10.1017/s1473550404002149.
Pełny tekst źródłaKärkäs, Markus D. "Electrochemical strategies for C–H functionalization and C–N bond formation". Chemical Society Reviews 47, nr 15 (2018): 5786–865. http://dx.doi.org/10.1039/c7cs00619e.
Pełny tekst źródłaMöhlmann, Lennart, Moritz Baar, Julian Rieß, Markus Antonietti, Xinchen Wang i Siegfried Blechert. "Carbon Nitride-Catalyzed Photoredox CC Bond Formation with N-Aryltetrahydroisoquinolines". Advanced Synthesis & Catalysis 354, nr 10 (5.06.2012): 1909–13. http://dx.doi.org/10.1002/adsc.201100894.
Pełny tekst źródłaLi, Jing-Yuan, Qing-Wen Song, Kan Zhang i Ping Liu. "Catalytic Conversion of Carbon Dioxide through C-N Bond Formation". Molecules 24, nr 1 (5.01.2019): 182. http://dx.doi.org/10.3390/molecules24010182.
Pełny tekst źródłaKerru, Nagaraju, Suresh Maddila i Sreekantha B. Jonnalagadda. "Design of Carbon-carbon and Carbon-heteroatom Bond Formation Reactions under Green Conditions". Current Organic Chemistry 23, nr 28 (17.01.2020): 3154–90. http://dx.doi.org/10.2174/1385272823666191202105820.
Pełny tekst źródłaMoehlmann, Lennart, Moritz Baar, Julian Riess, Markus Antonietti, Xinchen Wang i Siegfried Blechert. "ChemInform Abstract: Carbon Nitride-Catalyzed Photoredox C-C Bond Formation with N-Aryltetrahydroisoquinolines." ChemInform 43, nr 50 (29.11.2012): no. http://dx.doi.org/10.1002/chin.201250155.
Pełny tekst źródłaKamanna, Kantharaju, i Santosh Y. Khatavi. "Microwave-accelerated Carbon-carbon and Carbon-heteroatom Bond Formation via Multi-component Reactions: A Brief Overview". Current Microwave Chemistry 7, nr 1 (23.06.2020): 23–39. http://dx.doi.org/10.2174/2213346107666200218124147.
Pełny tekst źródłaYang, Zhen-Zhen, Liang-Nian He, Jiao Gao, An-Hua Liu i Bing Yu. "Carbon dioxide utilization with C–N bond formation: carbon dioxide capture and subsequent conversion". Energy & Environmental Science 5, nr 5 (2012): 6602. http://dx.doi.org/10.1039/c2ee02774g.
Pełny tekst źródłaCurrie, Lucy, Luca Rocchigiani, David L. Hughes i Manfred Bochmann. "Carbon–sulfur bond formation by reductive elimination of gold(iii) thiolates". Dalton Transactions 47, nr 18 (2018): 6333–43. http://dx.doi.org/10.1039/c8dt00906f.
Pełny tekst źródłaNi, Jing, i Xi Ping Hao. "Carbon Nitride Films Prepared by PECVD in CH4-NH3 Precursor". Advanced Materials Research 538-541 (czerwiec 2012): 124–27. http://dx.doi.org/10.4028/www.scientific.net/amr.538-541.124.
Pełny tekst źródłaRozprawy doktorskie na temat "Carbon-Nitrozen bond(C-N) formation"
Chakraborty, Rakesh Ranjan. "Explorative studies on carbon-nitrogen (C-N) bond formation and synthesis of nitrogen containing heterocyclic compounds". Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2798.
Pełny tekst źródłaDabb, Serin Lloyd Chemistry Faculty of Science UNSW. "Hydrazine in late transition metal-mediated N-C bond formation". Publisher:University of New South Wales. Chemistry, 2008. http://handle.unsw.edu.au/1959.4/41428.
Pełny tekst źródłaCai, Yingxiao. "Cobalt-catalyzed carbon-carbon bond formation by activation of carbon-halogen or carbon-hydrogen bonds". Thesis, Université Paris-Saclay (ComUE), 2016. http://www.theses.fr/2016SACLX039/document.
Pełny tekst źródłaThis thesis presents the development of cobalt-catalyzed carbon-carbon bonds formation. The first chapter describes a novel cobalt-catalyzed electrophilic cyanation of arylzinc species, employing benign and non-toxic N-cyano-N-phenyl-p-methylbenzenesulfonamide (NCTS) as the cyano source. In this reaction, cobalt catalyzes both the formation of arylzinc species and the cyanation reaction. Various benzonitriles are synthesized affording good to excellent yields. Using cobalt-bipyridine complexes instead of CoBr2, ketone and nitrile groups can be tolerated. The second chapter reports cobalt-catalyzed Csp3-Csp3 homocoupling reaction. A simple catalytic system could deliver dimers of a number of alkyl halides/pseudohalides and allylic acetates. Sodium iodide is crucial for the homocoupling of unactivated alkyl chlorides and tosylates. This method is extended to alkyl-alkyl cross-coupling; however, the conditions still need to be optimized. The third chapter describes a cobalt-catalyzed vinyl-benzyl cross-coupling. A variety of functionalized vinyl bromides and benzyl chlorides are efficiently coupled under mild conditions in good to excellent yields, with retention of Z/E configuration. A few mechanistic experiments indicate a single electron transfer involved. The last chapter discusses the progress on the cobalt-catalyzed arylation of 2-phenylpyridine with an arylzinc species by C-H activation and promising results are obtained
Ebe, Yusuke. "Iridium-Catalyzed Carbon-Carbon Bond Formation Reactions via C-H Bond Activation". 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225417.
Pełny tekst źródłaArambasic, Milan. "Carbon-carbon bond formation via rhodium-catalysed C-S activation processes". Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:e9e29a73-e637-4844-9a37-58b5ae4a3f99.
Pełny tekst źródłaSirokman, Gergely. "(N-heterocyclic-carbene)Copper(I)-catalyzed carbon-carbon bond formation using carbon dioxide". Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/39584.
Pełny tekst źródłaVita.
Includes bibliographical references.
This thesis presents work towards the development of a new catalytic C-C bond forming reaction. Alkynes and olefins insert into [(IPr)CuH]2 (IPr = N,N-bis-(2,6-diisopropylphenyl)-1,3-imidazol-2-ylidene) to give copper vinyl and copper alkyl complexes. These copper complexes insert CO2 into the Cu-C bond to form copper acrylate and copper carboxylate complexes. Acrylic and carboxylic acids can be isolated by hydrolysis. A catalytic cycle based on (IPr)copper(I) was developed. Alkynes undergo reductive carboxylation to give acrylic acids in moderate yields. Unexpected interactions between several components of the catalytic system led to a number of side reaction, most importantly between [(IPr)CuH]2 and the product silyl acrylate. The use of silylcarbonate salts to desylilate the product enhanced yield. In addition, silylcarbonates can also serve as a source of CO2.
by Gergely Sirokman.
Ph.D.
Masuda, Yuusuke. "Development of New C-C Bond Forming Reactions Utilizing Light as Energy Source". 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225634.
Pełny tekst źródłaHeckler, James E. "Advances in gold-carbon bond formation: mono-, di-, and triaurated organometallics". Case Western Reserve University School of Graduate Studies / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=case1441363597.
Pełny tekst źródłaKunchithapatham, Kamala. "Development of Calcium and Palladium Catalysts for the Formation of Carbon-Carbon and Carbon-Heteroatom Bonds". The Ohio State University, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=osu1337955731.
Pełny tekst źródłaBurgener, Simon [Verfasser], i Tobias Jürgen [Akademischer Betreuer] Erb. "Expanding the repertoire of enzymatic C-C bond formation with one-carbon units / Simon Burgener ; Betreuer: Tobias Jürgen Erb". Marburg : Philipps-Universität Marburg, 2021. http://d-nb.info/1239239890/34.
Pełny tekst źródłaKsiążki na temat "Carbon-Nitrozen bond(C-N) formation"
C-X bond formation. Heidelberg: Springer, 2010.
Znajdź pełny tekst źródłaVigalok, Arkadi. C-X Bond Formation. Springer, 2012.
Znajdź pełny tekst źródłaTaber, Douglass F., i Tristan Lambert. Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.001.0001.
Pełny tekst źródłaCzęści książek na temat "Carbon-Nitrozen bond(C-N) formation"
Wolfe, John P., Joshua D. Neukom i Duy H. Mai. "Synthesis of Saturated Five-Membered Nitrogen Heterocycles via Pd-Catalyzed CN Bond-Forming Reactions". W Catalyzed Carbon-Heteroatom Bond Formation, 1–34. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch1.
Pełny tekst źródłaSong, Qing-Wen, i Liang-Nian He. "Heterocyclic Synthesis Through C-N Bond Formation with Carbon Dioxide". W Chemistry Beyond Chlorine, 435–53. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30073-3_16.
Pełny tekst źródłaBichler, Paul, i Jennifer A. Love. "Organometallic Approaches to Carbon–Sulfur Bond Formation". W C-X Bond Formation, 39–64. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-12073-2_3.
Pełny tekst źródłaVigalok, Arkadi, i Ariela W. Kaspi. "Late Transition Metal-Mediated Formation of Carbon–Halogen Bonds". W C-X Bond Formation, 19–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-12073-2_2.
Pełny tekst źródłaWidenhoefer, Ross A., i Feijie Song. "Gold-Catalyzed Addition of Oxygen Nucleophiles to CC Multiple Bonds". W Catalyzed Carbon-Heteroatom Bond Formation, 463–92. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch12.
Pełny tekst źródłaLebel, Hélène. "Rhodium-Catalyzed CH Aminations". W Catalyzed Carbon-Heteroatom Bond Formation, 137–55. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch5.
Pełny tekst źródłaWidenhoefer, Ross A., i Feijie Song. "Gold-Catalyzed Addition of Nitrogen and Sulfur Nucleophiles to CC Multiple Bonds". W Catalyzed Carbon-Heteroatom Bond Formation, 437–61. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch11.
Pełny tekst źródłaYeung, Charles S., Peter K. Dornan i Vy M. Dong. "Transition Metal Catalyzed Approaches to Lactones Involving CO Bond Formation". W Catalyzed Carbon-Heteroatom Bond Formation, 35–68. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch2.
Pełny tekst źródłaHoberg, Heinz. "Stoichiometric Reactions of C-C Bond Formation Promoted by Metal Systems". W Carbon Dioxide as a Source of Carbon, 275–93. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3923-3_15.
Pełny tekst źródłaBae, Chulsung. "Catalytic Carbon–Boron Bond Formation via Activation of Alkane C–H Bonds". W Catalysis by Metal Complexes, 73–111. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-3698-8_3.
Pełny tekst źródłaStreszczenia konferencji na temat "Carbon-Nitrozen bond(C-N) formation"
Sahu, Sunil, Anil Tyagi, Yonghwee Kim i Arjun Puri. "Accurate Identification of Gas-Bearing Formation in a Mature Field Using Pulsed Neutron Logs Prevented Well Abandonment". W Gas & Oil Technology Showcase and Conference. SPE, 2023. http://dx.doi.org/10.2118/214153-ms.
Pełny tekst źródłaIvanova, M. S., M. V. Vishnetskaya i K. O. Tomsky. "Kinetics of carbon dioxide absorption and C-C bond formation in media containing trifluoroacetic acid". W ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0070381.
Pełny tekst źródłaAcquaviva, S., E. D’Anna, M. L. De Giorgi, G. Leggieri, A. Luches, M. Martino, A. Perrone i A. Zocco. "Carbon Nitride Films Synthesis and Deposition by Excimer Laser Ablation of Graphite Targets in Nitrogen Atmosphere". W The European Conference on Lasers and Electro-Optics. Washington, D.C.: Optica Publishing Group, 1998. http://dx.doi.org/10.1364/cleo_europe.1998.cmf3.
Pełny tekst źródłaAkram, M. Zuhaib, Yangbo Deng, Muhammad Aziz, Bingquan Ge i Hao Jiang. "<bold>NH</bold> <sub> <bold>3</bold> </sub> <bold>Impact on Combustion and Emission Characteristics of N-Heptane Flame</bold>". W WCX SAE World Congress Experience. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2023. http://dx.doi.org/10.4271/2023-01-0329.
Pełny tekst źródłaBolotov, Vasiliy Alexandrovich, Serguei Fedorovich Tikhov, Konstantin Radikovich Valeev, Vladimir Timurovich Shamirzaev i Valentin Nikolaevich Parmon. "SELECTIVE FORMATION OF LINEAR ALPHA-OLEFINS VIA MICROWAVE CATALYTIC CRACKING OF LIQUID STRAIGHT-CHAIN ALKANES". W Ampere 2019. Valencia: Universitat Politècnica de València, 2019. http://dx.doi.org/10.4995/ampere2019.2019.9894.
Pełny tekst źródłaNarumanchi, Sreekant, Douglas DeVoto, Mark Mihalic, Tim Popp i Patrick McCluskey. "Thermal Performance and Reliability of Large-Area Bonded Interfaces in Power Electronics Packages". W ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-65399.
Pełny tekst źródłaKumar, Anand, i Anchu Ashok. "Catalytic Decomposition of Ethanol over Bimetallic Nico Catalysts for Carbon Nanotube Synthesis". W Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2020. http://dx.doi.org/10.29117/quarfe.2020.0039.
Pełny tekst źródłaAikman, Michael John Lundin. "Clean Energy from Oil: A Process to Generate Low Cost, Low Carbon Electricity from Mature and Depleted Oil Fields". W ADIPEC. SPE, 2022. http://dx.doi.org/10.2118/210940-ms.
Pełny tekst źródłaYang, Silin, Ahmed Raslan, Antoine Durocher, Felix Güthe i Jeffrey Bergthorson. "Numerical Investigation of NH3 Doped Fuels From Biomass Gasification on Fuel-Bound NOx Formation at Gas Turbine Conditions". W ASME Turbo Expo 2023: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/gt2023-103191.
Pełny tekst źródłaSabet, Seyed Morteza, Hassan Mahfuz, Andrew C. Terentis i Javad Hashemi. "A New Approach to the Synthesis of Carbon Nanotube-Polyhedral Oligomeric Silsesquioxane (POSS) Nanohybrids". W ASME 2015 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/imece2015-50925.
Pełny tekst źródłaRaporty organizacyjne na temat "Carbon-Nitrozen bond(C-N) formation"
Shomer, Ilan, Ruth E. Stark, Victor Gaba i James D. Batteas. Understanding the hardening syndrome of potato (Solanum tuberosum L.) tuber tissue to eliminate textural defects in fresh and fresh-peeled/cut products. United States Department of Agriculture, listopad 2002. http://dx.doi.org/10.32747/2002.7587238.bard.
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