Gotowa bibliografia na temat „Bond forming”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Spis treści
Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Bond forming”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Artykuły w czasopismach na temat "Bond forming"
Dyball, H. "Forming a bond". Electronics Letters 46, nr 14 (2010): 962. http://dx.doi.org/10.1049/el.2010.9086.
Pełny tekst źródłaDay, Lin. "Forming a loving bond". Early Years Educator 10, nr 2 (czerwiec 2008): 32–34. http://dx.doi.org/10.12968/eyed.2008.10.2.29168.
Pełny tekst źródłaMague, Joel T., Alaa A. M. Abdel-Aziz, Adel S. El-Azab i Amer M. Alanazi. "1-Acetyl-5-methoxy-4-(phenylsulfanyl)imidazolidin-2-one". Acta Crystallographica Section E Structure Reports Online 70, nr 2 (15.01.2014): o145—o146. http://dx.doi.org/10.1107/s1600536814000117.
Pełny tekst źródłaFujii, Isao. "Crystal structure of (S)-2-amino-2-methylsuccinic acid". Acta Crystallographica Section E Crystallographic Communications 71, nr 10 (12.09.2015): o731—o732. http://dx.doi.org/10.1107/s2056989015016709.
Pełny tekst źródłaGreen, Nicholas J., i Michael S. Sherburn. "Multi-Bond Forming Processes in Efficient Synthesis". Australian Journal of Chemistry 66, nr 3 (2013): 267. http://dx.doi.org/10.1071/ch13003.
Pełny tekst źródłaGagné, Olivier Charles, Patrick H. J. Mercier i 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, nr 6 (1.12.2018): 470–82. http://dx.doi.org/10.1107/s2052520618010442.
Pełny tekst źródłaReardon-Robinson, Melissa E., i Hung Ton-That. "Disulfide-Bond-Forming Pathways in Gram-Positive Bacteria". Journal of Bacteriology 198, nr 5 (7.12.2015): 746–54. http://dx.doi.org/10.1128/jb.00769-15.
Pełny tekst źródłaMoriguchi, Tetsuji, Venkataprasad Jalli, Suvratha Krishnamurthy, Akihiko Tsuge i 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, nr 12 (1.12.2015): o1049—o1050. http://dx.doi.org/10.1107/s2056989015023592.
Pełny tekst źródłaCurtis, Richard, R. Omar, J. Bahra, M. Ditta, A. Chotai i Lucy DiSilvio. "Superplastic Prosthetic Forming - In Vitro Response". Key Engineering Materials 433 (marzec 2010): 31–39. http://dx.doi.org/10.4028/www.scientific.net/kem.433.31.
Pełny tekst źródłaBegum, M. S., M. B. H. Howlader, M. C. Sheikh, R. Miyatake i E. Zangrando. "Crystal structure ofS-hexyl (E)-3-(2-hydroxybenzylidene)dithiocarbazate". Acta Crystallographica Section E Crystallographic Communications 72, nr 3 (6.02.2016): 290–92. http://dx.doi.org/10.1107/s2056989016001857.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaCommittee 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.
Pełny tekst źródłaLa 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.
Pełny tekst źródłaMori-Quiroz, Luis Martin. "Transition metal catalyzed Carbon-nitrogen bond forming reactions". Revista de Química, 2015. http://repositorio.pucp.edu.pe/index/handle/123456789/101381.
Pełny tekst źródłaCarbon-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.
Pełny tekst źródłaHughes, 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.
Pełny tekst źródłaLomas, 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.
Pełny tekst źródłaTundel, 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.
Pełny tekst źródłaVita. 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.
Pełny tekst źródłaBrace, 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.
Pełny tekst źródłaKsiążki na temat "Bond forming"
M, Roberts Stanley, red. Metal catalysed carbon-carbon bond-forming reactions. Chichester, West Sussex, England: John Wiley, 2004.
Znajdź pełny tekst źródłaRodriguez, Jean, i 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.
Pełny tekst źródłaRodriguez, Jean, i Damien Bonne. Stereoselective multiple bond-forming transformations in organic synthesis. Hoboken, New Jersey: John Wiley & Sons, Inc., 2015.
Znajdź pełny tekst źródłaRoberts, Stanley M., Jianliang Xiao, John Whittall i Tom E. Pickett, red. 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.
Pełny tekst źródłaTechnical Association of the Pulp and Paper Industry, Engineering Conference (1997 : Nashville, Tenn.) i Papermakers Conference (1997 : Nashville, Tenn.), red. Engineering & papermakers: Forming bonds for better papermaking : October 6-9, 1997, Opryland Hotel, Nashville, TN. Atlanta, GA: TAPPI Press, 1997.
Znajdź pełny tekst źródłaDanheiser, Rick L. Asymmetric Carbon-Carbon Bond Forming Reactions. Wiley & Sons, Incorporated, John, 2018.
Znajdź pełny tekst źródłaRoberts, Stanley M., John Whittall, Jianliang Xiao i Tom E. Pickett. Metal Catalysed Carbon-Carbon Bond-Forming Reactions. Wiley & Sons, Incorporated, John, 2007.
Znajdź pełny tekst źródłaSharma, Rakesh Kumar, i Bubun Banerjee. [Set Green-Bond Forming Reactions, Vol 1+2]. de Gruyter GmbH, Walter, 2022.
Znajdź pełny tekst źródłaEnders, Dieter, Jean Rodriguez i Damien Bonne. Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.
Znajdź pełny tekst źródłaEnders, Dieter, Jean Rodriguez i Damien Bonne. Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis. Wiley & Sons, Limited, John, 2015.
Znajdź pełny tekst źródłaCzęści książek na temat "Bond forming"
Sun, Chang Q. "Kinetics of Bond Forming and Bond Switching". W Springer Series in Chemical Physics, 147–51. Singapore: Springer Singapore, 2014. http://dx.doi.org/10.1007/978-981-4585-21-7_7.
Pełny tekst źródłaZhdankin, Viktor V. "C-C-Bond Forming Reactions". W Hypervalent Iodine Chemistry, 99–136. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_4.
Pełny tekst źródłaKoser, Gerald F. "C-Heteroatom-Bond Forming Reactions". W Hypervalent Iodine Chemistry, 137–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_5.
Pełny tekst źródłaKoser, Gerald F. "Heteroatom-Heteroatom-Bond Forming Reactions". W Hypervalent Iodine Chemistry, 173–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_6.
Pełny tekst źródłaAtta-ur-Rahman i Zahir Shah. "Stereoselective Carbon-Carbon Bond Forming Reactions". W 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.
Pełny tekst źródłaShimizu, Masaki. "CC Bond-Forming Coupling Reactions". W Transition-Metal-Mediated Aromatic Ring Construction, 571–616. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch22.
Pełny tekst źródłaParashar, Rakesh Kumar. "Carbon-Carbon Double Bond Forming Reactions". W Reaction Mechanisms in Organic Synthesis, 148–90. West Sussex, United Kingdom: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118681299.ch4.
Pełny tekst źródłaBonne, Damien, Thierry Constantieux, Yoann Coquerel i Jean Rodriguez. "Cascade Reactions Forming Both C-C Bond and C-Heteroatom BOND". W Stereoselective Organocatalysis, 559–85. Hoboken, New Jersey: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118604755.ch16.
Pełny tekst źródłaZarganes-Tzitzikas, Tryfon, Ahmad Yazbak i Alexander Dömling. "Industrial Applications of Multiple Bond-Forming Transformations (MBFTs)". W 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.
Pełny tekst źródłaParashar, Rakesh Kumar. "Transition Metal-Mediated Carbon-Carbon Bond Forming Reactions". W Reaction Mechanisms in Organic Synthesis, 191–223. West Sussex, United Kingdom: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118681299.ch5.
Pełny tekst źródłaStreszczenia konferencji na temat "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". W Material Forming. Materials Research Forum LLC, 2024. http://dx.doi.org/10.21741/9781644903131-87.
Pełny tekst źródłaDENKENA, B. "Manufacturing of graded grinding wheels for flute grinding". W Material Forming. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902479-132.
Pełny tekst źródłaPIWEK, A. "Investigation of the joining zone formation of impact extruded hybrid components by varied forming sequence and partial cooling". W Material Forming. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902479-64.
Pełny tekst źródłaSIEGMUND, M. "Hot die forging with nitrided and thermally stabilized DLC coated tools". W Material Forming. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902479-63.
Pełny tekst źródłaKAUSHIK, Pankaj. "Friction stir-assisted cladding: Solid-state recycling of machine shop scrap for sustainable metal production". W Material Forming. Materials Research Forum LLC, 2024. http://dx.doi.org/10.21741/9781644903131-309.
Pełny tekst źródłaBiresaw, Girma, Terry A. Isbell i Steven C. Cermak. "Film-Forming Properties of Estolides". W World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-64089.
Pełny tekst źródłaKhaledi, Kavan, Stephan Wulfinghoff i Stefanie Reese. "Analysis of factors influencing the bond strength in roll bonding processes". W PROCEEDINGS OF THE 21ST INTERNATIONAL ESAFORM CONFERENCE ON MATERIAL FORMING: ESAFORM 2018. Author(s), 2018. http://dx.doi.org/10.1063/1.5034863.
Pełny tekst źródłaUbani, Solomon, Muhannad A. Obeidi i Dermot Brabazon. "Laser surface texturing for the improvement of press-fit joint bond strength". W PROCEEDINGS OF THE 22ND INTERNATIONAL ESAFORM CONFERENCE ON MATERIAL FORMING: ESAFORM 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5112689.
Pełny tekst źródłaWang, Xueqiang, Joan G. Donaire i Ruben Martin. "Metal-Free sp2 and sp3 C-H Functionalization/C-O Bond Forming Reaction". W 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013815132216.
Pełny tekst źródłaChen, Jau-Liang, Yeh-Chao Lin, Chun-Hsien Liu, Wen-Chang Kuo i Tzung-Ching Lee. "Application of Neural Network in Free Air Ball Forming for Wire Bonder". W ASME 1999 Design Engineering Technical Conferences. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/detc99/cie-9087.
Pełny tekst źródłaRaporty organizacyjne na temat "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), wrzesień 2002. http://dx.doi.org/10.2172/803353.
Pełny tekst źródłaCohen, William S. Defense Issue: Volume 13, Number 27. Forming Bonds of Diplomacy to Avoid War. Fort Belvoir, VA: Defense Technical Information Center, marzec 1998. http://dx.doi.org/10.21236/ada342485.
Pełny tekst źródłaRiveros, Guillermo, Felipe Acosta, Reena Patel i Wayne Hodo. Computational mechanics of the paddlefish rostrum. Engineer Research and Development Center (U.S.), wrzesień 2021. http://dx.doi.org/10.21079/11681/41860.
Pełny tekst źródła