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Статті в журналах з теми "Bond forming"
Dyball, H. "Forming a bond." Electronics Letters 46, no. 14 (2010): 962. http://dx.doi.org/10.1049/el.2010.9086.
Повний текст джерелаDay, Lin. "Forming a loving bond." Early Years Educator 10, no. 2 (June 2008): 32–34. http://dx.doi.org/10.12968/eyed.2008.10.2.29168.
Повний текст джерелаMague, Joel T., Alaa A. M. Abdel-Aziz, Adel S. El-Azab, and Amer M. Alanazi. "1-Acetyl-5-methoxy-4-(phenylsulfanyl)imidazolidin-2-one." Acta Crystallographica Section E Structure Reports Online 70, no. 2 (January 15, 2014): o145—o146. http://dx.doi.org/10.1107/s1600536814000117.
Повний текст джерелаFujii, Isao. "Crystal structure of (S)-2-amino-2-methylsuccinic acid." Acta Crystallographica Section E Crystallographic Communications 71, no. 10 (September 12, 2015): o731—o732. http://dx.doi.org/10.1107/s2056989015016709.
Повний текст джерелаGreen, Nicholas J., and Michael S. Sherburn. "Multi-Bond Forming Processes in Efficient Synthesis." Australian Journal of Chemistry 66, no. 3 (2013): 267. http://dx.doi.org/10.1071/ch13003.
Повний текст джерелаGagné, Olivier Charles, Patrick H. J. Mercier, and Frank Christopher Hawthorne. "A priori bond-valence and bond-length calculations in rock-forming minerals." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 74, no. 6 (December 1, 2018): 470–82. http://dx.doi.org/10.1107/s2052520618010442.
Повний текст джерелаReardon-Robinson, Melissa E., and Hung Ton-That. "Disulfide-Bond-Forming Pathways in Gram-Positive Bacteria." Journal of Bacteriology 198, no. 5 (December 7, 2015): 746–54. http://dx.doi.org/10.1128/jb.00769-15.
Повний текст джерелаMoriguchi, Tetsuji, Venkataprasad Jalli, Suvratha Krishnamurthy, Akihiko Tsuge, and Kenji Yoza. "Crystal structure of ethyl 2-(2-{1-[N-(4-bromophenyl)-2-oxo-2-phenylacetamido]-2-tert-butylamino-2-oxoethyl}-1H-pyrrol-1-yl)acetate." Acta Crystallographica Section E Crystallographic Communications 71, no. 12 (December 1, 2015): o1049—o1050. http://dx.doi.org/10.1107/s2056989015023592.
Повний текст джерелаCurtis, Richard, R. Omar, J. Bahra, M. Ditta, A. Chotai, and Lucy DiSilvio. "Superplastic Prosthetic Forming - In Vitro Response." Key Engineering Materials 433 (March 2010): 31–39. http://dx.doi.org/10.4028/www.scientific.net/kem.433.31.
Повний текст джерелаBegum, M. S., M. B. H. Howlader, M. C. Sheikh, R. Miyatake, and E. Zangrando. "Crystal structure ofS-hexyl (E)-3-(2-hydroxybenzylidene)dithiocarbazate." Acta Crystallographica Section E Crystallographic Communications 72, no. 3 (February 6, 2016): 290–92. http://dx.doi.org/10.1107/s2056989016001857.
Повний текст джерелаДисертації з теми "Bond forming"
Hoskins, Travis Justin Christopher. "Carbon-carbon bond forming reactions." Thesis, Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/29769.
Повний текст джерелаCommittee Chair: Dr. Christopher Jones; Committee Co-Chair: Dr. Pradeep Agrawal; Committee Member: Dr. Sujit Banerjee; Committee Member: Dr. Tom Fuller. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Buzzetti, Luca. "Photochemical Strategies for Carbon–Carbon Bond Forming Processes." Doctoral thesis, Universitat Rovira i Virgili, 2018. http://hdl.handle.net/10803/668971.
Повний текст джерелаLa capacidad de generar intermedios radicalarios, bajo condiciones suaves, ha llevado al emergente campo de la catálisis fotoredox al desarrollo de nuevas transformaciones. Tradicionalmente, esta se basa en el uso de un fotocatalizador, que absorbe eficientemente luz e induce una transferencia simple de electrones (SET). Sin embargo, la reactividad química de las moléculas excitadas electrónicamente difiere fundamentalmente de las que se encuentran en su estado fundamental. Una molécula en estado excitado es a la vez una mejor donante y aceptora de electrones que en su estado fundamental y se comporta respectivamente como una mejor reductora y una mejor oxidante. El principal objetivo científico de esta tesis doctoral ha sido investigar y comprender la reactividad del estado excitado de algunas moléculas orgánicas para desarrollar nuevos procesos fotoquímicos de formación de enlaces C-C. Para lograr este objetivo, se han combinado diferentes herramientas de la química orgánica. En los primeros proyectos (discutidos en los Capítulos III y IV), la fusión de la organocatálisis y la fotoquímica han permitido la funcionalización asimétrica directa en la posición β de enales, desencadenada por la excitación con luz visible de sales de iminio quirales formadas in situ. En la segunda parte de estos estudios doctorales (discutido en el Capítulo V), se ha explotado las propiedades del estado excitado de 4-alquil-1,4-dihidropiridinas (alquil-DHP) en combinación con la catálisis de metales de transición para el desarrollo de catalizadores de níquel en reacciones radicalarias de acoplamiento cruzado.
The emerging field of photoredox catalysis has led to the development of new transformations due to the ability to generate radical intermediates under mild conditions. Traditionally, this relies on the use of a photocatalyst, which efficiently absorbs light and induces a single electron transfer (SET). However, the chemical reactivity of electronically excited molecules differs fundamentally from that in the ground state. An excited-state molecule is both a better electron donor and a better electron acceptor than in the ground state and behaves respectively as a better reductant and a better oxidant. The main scientific objective of this doctoral research was to investigate and understand the excited-state reactivity of some organic molecules to develop novel photochemical C–C bond-forming processes. In order to achieve this goal, different tools of organic chemistry were combined. In the first projects (discussed in Chapter III and IV), the merger of organocatalysis and photochemistry enabled the direct asymmetric β-functionalization of enals triggered by the visible-light excitation of in situ formed chiral iminium salts. In the second part of the PhD studies (discussed in Chapter V), the excited-state properties of 4-alkyl-1,4-dihydropyridines (alkyl-DHP) were exploited in combination with transition metal catalysis for the development of nickel-catalyzed radical cross-couplings.
Bentz, Emilie Louise Marie. "Zinc enolate coupling : carbon-carbon bond forming reactions." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419263.
Повний текст джерелаMori-Quiroz, Luis Martin. "Transition metal catalyzed Carbon-nitrogen bond forming reactions." Revista de Química, 2015. http://repositorio.pucp.edu.pe/index/handle/123456789/101381.
Повний текст джерелаCarbon-nitrogen (C–N) bond forming reactions are fundamental transformations in nature and also basic processes for the preparation of molecules and materials relevant to human activities. The development of new and efficient reactions for the formation of C–N bonds are therefore of great interest in academic and industrial settings. Progress in the last 20 years has focused mainly in Csp2–N bond forming processes; however, there is growing range of transition metal catalyzed reactions for the introduction of nitrogen in alkyl frameworks (Csp3–N bond formation). This article describes a selection of modern catalytic methods for the formation of C–N bonds.
Pilarski, Lukasz T. "Palladacycles for non-redox C-C bond forming reactions." Thesis, University of Bristol, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.495644.
Повний текст джерелаHughes, Steven P. "Studies in bond-forming reactions of alpha-lithiated aziridines." Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.496916.
Повний текст джерелаLomas, Sarah. "C-C bond forming catalysis with alkaline earth acetylides." Thesis, University of Bath, 2013. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.604644.
Повний текст джерелаTundel, Rachel E. (Rachel Elizabeth). "Advances in palladium-catalyzed carbon-nitrogen bond forming processes." Thesis, Massachusetts Institute of Technology, 2006. http://hdl.handle.net/1721.1/36283.
Повний текст джерелаVita. Leaf 68 blank.
Includes bibliographical references.
Chapter 1. Microwave-assisted, palladium-catalyzed C-N bond-forming reactions with aryl/heteroaryl nonaflates/halides and amines using the soluble amine bases DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) or MTBD (7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene) and a catalyst system consisting of Pd2dba3 and ligands (XantPhos, 2-dicylcohexylphosphino-2',4',6'-triisopropyl-1,1 '-biphenyl (XPhos) and 2-di-tert-butylphosphino-2',4',6'-triisopropyl-1, '-biphenyl) resulted in good to excellent yields of arylamines in short reaction times. Chapter 2. Using a catalyst comprised of the bulky, electron-rich monophosphine ligand di-tert-Butyl XPhos (2-di-tert-butylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl) and Pd2dba3 with sodium tert-butoxide as the base, amino heterocycles were coupled successfully with aryl/heteroaryl halides in moderate to excellent yields.
by Rachel E. Tundel.
S.B.
Gates, Bradley Durward. "Novel thermal and electrochemical carbon-carbon bond-forming reactions /." The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487847761307998.
Повний текст джерелаBrace, Gareth Neil. "Applications of palladium-catalysed C-N bond forming reactions." Thesis, University of Bath, 2006. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.428381.
Повний текст джерелаКниги з теми "Bond forming"
M, Roberts Stanley, ed. Metal catalysed carbon-carbon bond-forming reactions. Chichester, West Sussex, England: John Wiley, 2004.
Знайти повний текст джерелаRodriguez, Jean, and Damien Bonne. Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. Hoboken, NJ, USA: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119006220.
Повний текст джерелаRodriguez, Jean, and Damien Bonne. Stereoselective multiple bond-forming transformations in organic synthesis. Hoboken, New Jersey: John Wiley & Sons, Inc., 2015.
Знайти повний текст джерелаRoberts, Stanley M., Jianliang Xiao, John Whittall, and Tom E. Pickett, eds. Catalysts for Fine Chemical Synthesis, Volume 3, Metal Catalysed Carbon-Carbon Bond-Forming Reactions. Chichester, UK: John Wiley & Sons, Ltd, 2004. http://dx.doi.org/10.1002/0470862017.
Повний текст джерелаTechnical Association of the Pulp and Paper Industry, Engineering Conference (1997 : Nashville, Tenn.), and Papermakers Conference (1997 : Nashville, Tenn.), eds. Engineering & papermakers: Forming bonds for better papermaking : October 6-9, 1997, Opryland Hotel, Nashville, TN. Atlanta, GA: TAPPI Press, 1997.
Знайти повний текст джерелаDanheiser, Rick L. Asymmetric Carbon-Carbon Bond Forming Reactions. Wiley & Sons, Incorporated, John, 2018.
Знайти повний текст джерелаRoberts, Stanley M., John Whittall, Jianliang Xiao, and Tom E. Pickett. Metal Catalysed Carbon-Carbon Bond-Forming Reactions. Wiley & Sons, Incorporated, John, 2007.
Знайти повний текст джерелаSharma, Rakesh Kumar, and Bubun Banerjee. [Set Green-Bond Forming Reactions, Vol 1+2]. de Gruyter GmbH, Walter, 2022.
Знайти повний текст джерелаEnders, Dieter, Jean Rodriguez, and Damien Bonne. Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.
Знайти повний текст джерелаEnders, Dieter, Jean Rodriguez, and Damien Bonne. Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. Wiley & Sons, Limited, John, 2015.
Знайти повний текст джерелаЧастини книг з теми "Bond forming"
Sun, Chang Q. "Kinetics of Bond Forming and Bond Switching." In Springer Series in Chemical Physics, 147–51. Singapore: Springer Singapore, 2014. http://dx.doi.org/10.1007/978-981-4585-21-7_7.
Повний текст джерелаZhdankin, Viktor V. "C-C-Bond Forming Reactions." In Hypervalent Iodine Chemistry, 99–136. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_4.
Повний текст джерелаKoser, Gerald F. "C-Heteroatom-Bond Forming Reactions." In Hypervalent Iodine Chemistry, 137–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_5.
Повний текст джерелаKoser, Gerald F. "Heteroatom-Heteroatom-Bond Forming Reactions." In Hypervalent Iodine Chemistry, 173–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_6.
Повний текст джерелаAtta-ur-Rahman and Zahir Shah. "Stereoselective Carbon-Carbon Bond Forming Reactions." In Stereoselective Synthesis in Organic Chemistry, 185–396. New York, NY: Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4613-8327-7_4.
Повний текст джерелаShimizu, Masaki. "CC Bond-Forming Coupling Reactions." In Transition-Metal-Mediated Aromatic Ring Construction, 571–616. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch22.
Повний текст джерелаParashar, Rakesh Kumar. "Carbon-Carbon Double Bond Forming Reactions." In Reaction Mechanisms in Organic Synthesis, 148–90. West Sussex, United Kingdom: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118681299.ch4.
Повний текст джерелаBonne, Damien, Thierry Constantieux, Yoann Coquerel, and Jean Rodriguez. "Cascade Reactions Forming Both C-C Bond and C-Heteroatom BOND." In Stereoselective Organocatalysis, 559–85. Hoboken, New Jersey: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118604755.ch16.
Повний текст джерелаZarganes-Tzitzikas, Tryfon, Ahmad Yazbak, and Alexander Dömling. "Industrial Applications of Multiple Bond-Forming Transformations (MBFTs)." In Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis, 423–46. Hoboken, NJ, USA: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119006220.ch15.
Повний текст джерелаParashar, Rakesh Kumar. "Transition Metal-Mediated Carbon-Carbon Bond Forming Reactions." In Reaction Mechanisms in Organic Synthesis, 191–223. West Sussex, United Kingdom: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118681299.ch5.
Повний текст джерелаТези доповідей конференцій з теми "Bond forming"
PIWEK, A. "Influence of enlarged joining zone interfaces on the bond properties of tailored formed hybrid components made of 20MnCr5 steel and EN AW-6082 aluminium." In Material Forming. Materials Research Forum LLC, 2024. http://dx.doi.org/10.21741/9781644903131-87.
Повний текст джерелаDENKENA, B. "Manufacturing of graded grinding wheels for flute grinding." In Material Forming. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902479-132.
Повний текст джерелаPIWEK, A. "Investigation of the joining zone formation of impact extruded hybrid components by varied forming sequence and partial cooling." In Material Forming. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902479-64.
Повний текст джерелаSIEGMUND, M. "Hot die forging with nitrided and thermally stabilized DLC coated tools." In Material Forming. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902479-63.
Повний текст джерелаKAUSHIK, Pankaj. "Friction stir-assisted cladding: Solid-state recycling of machine shop scrap for sustainable metal production." In Material Forming. Materials Research Forum LLC, 2024. http://dx.doi.org/10.21741/9781644903131-309.
Повний текст джерелаBiresaw, Girma, Terry A. Isbell, and Steven C. Cermak. "Film-Forming Properties of Estolides." In World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-64089.
Повний текст джерелаKhaledi, Kavan, Stephan Wulfinghoff, and Stefanie Reese. "Analysis of factors influencing the bond strength in roll bonding processes." In PROCEEDINGS OF THE 21ST INTERNATIONAL ESAFORM CONFERENCE ON MATERIAL FORMING: ESAFORM 2018. Author(s), 2018. http://dx.doi.org/10.1063/1.5034863.
Повний текст джерелаUbani, Solomon, Muhannad A. Obeidi, and Dermot Brabazon. "Laser surface texturing for the improvement of press-fit joint bond strength." In PROCEEDINGS OF THE 22ND INTERNATIONAL ESAFORM CONFERENCE ON MATERIAL FORMING: ESAFORM 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5112689.
Повний текст джерелаWang, Xueqiang, Joan G. Donaire, and Ruben Martin. "Metal-Free sp2 and sp3 C-H Functionalization/C-O Bond Forming Reaction." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013815132216.
Повний текст джерелаChen, Jau-Liang, Yeh-Chao Lin, Chun-Hsien Liu, Wen-Chang Kuo, and Tzung-Ching Lee. "Application of Neural Network in Free Air Ball Forming for Wire Bonder." In ASME 1999 Design Engineering Technical Conferences. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/detc99/cie-9087.
Повний текст джерелаЗвіти організацій з теми "Bond forming"
Templeton, J. L. Bond forming reactions of carbyne and nitrene complexes. Final technical report for DE-FG02-96ER14608. Office of Scientific and Technical Information (OSTI), September 2002. http://dx.doi.org/10.2172/803353.
Повний текст джерелаCohen, William S. Defense Issue: Volume 13, Number 27. Forming Bonds of Diplomacy to Avoid War. Fort Belvoir, VA: Defense Technical Information Center, March 1998. http://dx.doi.org/10.21236/ada342485.
Повний текст джерелаRiveros, Guillermo, Felipe Acosta, Reena Patel, and Wayne Hodo. Computational mechanics of the paddlefish rostrum. Engineer Research and Development Center (U.S.), September 2021. http://dx.doi.org/10.21079/11681/41860.
Повний текст джерела