Literatura académica sobre el tema "Transition-metal catalyzed organic transformations"
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Artículos de revistas sobre el tema "Transition-metal catalyzed organic transformations"
Mhaske, Santosh y Ranjeet Dhokale. "Transition-Metal-Catalyzed Reactions Involving Arynes". Synthesis 50, n.º 01 (22 de noviembre de 2017): 1–16. http://dx.doi.org/10.1055/s-0036-1589517.
Texto completoKuninobu, Yoichiro. "Transition Metal-Catalyzed Highly Efficient and Novel Transformations". Journal of Synthetic Organic Chemistry, Japan 71, n.º 5 (2013): 425–32. http://dx.doi.org/10.5059/yukigoseikyokaishi.71.425.
Texto completoTakacs, J. M., S. C. Boito y Y. C. Myoung. "Recent Applications of Catalytic Metal-Mediated Carbocyclizations in Asymmetric Synthesis". Current Organic Chemistry 2, n.º 3 (mayo de 1998): 233–54. http://dx.doi.org/10.2174/1385272802666220128192732.
Texto completoYuan, Jia, Ying Zhang, Hong Yu, Cuiying Wang, Sixuan Meng, Jian Chen, Guang-Ao Yu y Chi-Ming Che. "Transition metal complexes with functionalized indenyl phosphine ligands: structures and catalytic properties". Organic & Biomolecular Chemistry 20, n.º 3 (2022): 485–97. http://dx.doi.org/10.1039/d1ob01884a.
Texto completoZuo, Linhong, Teng Liu, Xiaowei Chang y Wusheng Guo. "An Update of Transition Metal-Catalyzed Decarboxylative Transformations of Cyclic Carbonates and Carbamates". Molecules 24, n.º 21 (31 de octubre de 2019): 3930. http://dx.doi.org/10.3390/molecules24213930.
Texto completoSala, Roberto, Camilla Loro, Francesca Foschi y Gianluigi Broggini. "Transition Metal Catalyzed Azidation Reactions". Catalysts 10, n.º 10 (12 de octubre de 2020): 1173. http://dx.doi.org/10.3390/catal10101173.
Texto completoXu, Qing, Changqiu Zhao, Yongbo Zhou, Shuangfeng Yin y Libiao Han. "Transition Metal-Catalyzed Transformations of P(O)—H Bonds". Chinese Journal of Organic Chemistry 32, n.º 10 (2012): 1761. http://dx.doi.org/10.6023/cjoc201207024.
Texto completoDella Ca’, Nicola. "Palladium-Catalyzed Reactions". Catalysts 11, n.º 5 (30 de abril de 2021): 588. http://dx.doi.org/10.3390/catal11050588.
Texto completoLandelle, Grégory, Armen Panossian, Sergiy Pazenok, Jean-Pierre Vors y Frédéric R. Leroux. "Recent advances in transition metal-catalyzed Csp2-monofluoro-, difluoro-, perfluoromethylation and trifluoromethylthiolation". Beilstein Journal of Organic Chemistry 9 (15 de noviembre de 2013): 2476–536. http://dx.doi.org/10.3762/bjoc.9.287.
Texto completoMarset, Xavier y Gabriela Guillena. "Deep Eutectic Solvents as à-la-Carte Medium for Transition-Metal-Catalyzed Organic Processes". Molecules 27, n.º 23 (2 de diciembre de 2022): 8445. http://dx.doi.org/10.3390/molecules27238445.
Texto completoTesis sobre el tema "Transition-metal catalyzed organic transformations"
Das, Pralay. "New reactions and methodology : studies on transition metal catalyzed organic transformations". Thesis, University of North Bengal, 2005. http://hdl.handle.net/123456789/775.
Texto completoGanguly, Bhaskar. "Transition-metal catalyzed organic transformations and application towards the synthesis of heterocyclic compounds". Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2650.
Texto completoGandolfo, Eugenio. "Light-driven Metal-catalyzed Asymmetric Transformations". Doctoral thesis, Universitat Rovira i Virgili, 2021. http://hdl.handle.net/10803/672439.
Texto completoResumen Una molécula en su estado excitado ofrece una reactividad completamente diferente a la de su estado fundamental. Puede comportarse tanto como mejor oxidante como mejor reductor, lo que permite nuevas transformaciones debido a la capacidad de generar radicales intermedios en condiciones suaves. El principal objetivo científico de esta tesis doctoral fue investigar la excitación directa de sustratos e intermedios de reacción para desbloquear nuevas formas de reacción, permitiendo transformaciones asimétricas catalizadas por metales las cuales serían inviables bajo el dominio térmico. Con este fin, investigué la química de las 4-alquil-1,4-dihidropiridinas (4-alquil-DHP) como fuente de electrones y precursores de radicales tanto en su estado excitado como en su estado fundamental. En el primer proyecto, aproveché las propiedades de los 4-alquil-DHP en su estado excitado, actuando como fuertes fotorreductores y fuente de radicales, para permitir el acoplamiento cruzado asimétrico de acilo catalizado con níquel y así, acceder a cetonas α, α-disustituidas altamente enantioenriquecidas. En el segundo proyecto, estudié cómo, mediante la excitación de la luz, era posible desviar la reactividad establecida en el estado fundamental de un complejo quiral de organoiridio, permitiendo procesos mecanísticos originales inalcanzables en el dominio térmico. En particular, probamos un complejo particular de η3-aliliridio (III) quiral para el cual estimamos un potencial de oxidación de ̴ +1.24 V en el estado excitado. Esta nueva función catalítica adquirida tras su excitación con la luz se aprovechó para desarrollar un acoplamiento cruzado enantioselectivo alquil-alquilo entre alcoholes bencil alílicos y radicales α-amino, derivados de 4-alquil-DHP que sirven como fuentes de radicales en estado fundamental.
Abstract An excited-state molecule offers a completely different reactivity than in its ground state. It can be both a better oxidant and a better reductant, thus enabling novel transformations due to the ability to generate radical intermediates under mild conditions. The main scientific objective of this doctoral thesis was to investigate the direct excitation of substrates and intermediates to unlock novel reactivity manifolds, enabling asymmetric metal-catalyzed transformations unfeasible under the thermal domain. To this end, I exploited the chemistry of 4-alkyl-1,4-dihydropyridines (4-alkyl-DHPs) in either their excited- and ground-state as sources of electrons and radical precursors. In the first project, I exploited the excited-state properties of 4-alkyl-DHPs, serving as strong photoreductant and radicals source, to enable an asymmetric nickel-catalyzed acyl cross-coupling to access highly enantioenriched α,α-disubstituted ketones. In the second project, I studied how, by means of light-excitation, it was possible to divert the established ground-state reactivity of an organoiridium chiral complex, enabling mechanistically original processes unattainable in the thermal domain. In particular, we probed a particular chiral η3-allyliridium(III) complex for which we estimated an oxidation potential of ̴ +1.24 V in the excited state. This novel catalytic function acquired upon light excitation was exploited to develop an enantioselective alkyl-alkyl cross-coupling between benzyl allylic alcohols and α-amino radicals, derived from 4-alkyl-DHPs serving as ground-state radical sources.
Nimmagadda, Sri Krishna. "Asymmetric Transformations Catalyzed By Chiral BINOL Alkaline Earth Metal Phosphate Complexes". Scholar Commons, 2016. http://scholarcommons.usf.edu/etd/6554.
Texto completoTan, Peng Wen. "Transition metal catalyzed reactions and functionalized group transformations". Thesis, University of Oxford, 2017. https://ora.ox.ac.uk/objects/uuid:336947d0-c3c7-4c45-9849-d3231c53ab42.
Texto completoSong, Xuejing. "Studies of transition metal catalyzed propylene polymerization". Thesis, University of Oxford, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308611.
Texto completoZweni, Pumza P. "Dendrimer-transition metal catalyzed oxidation and reduction reactions". Thesis, University of Ottawa (Canada), 2005. http://hdl.handle.net/10393/10529.
Texto completoTrono, Corazon. "Transition metal catalyzed synthesis of glycoclusters from sugar alkynes". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ58515.pdf.
Texto completoTatsumi, Kenta. "Transition Metal-Catalyzed Novel Transformations of Acid Chlorides and Acid Anhydrides". Kyoto University, 2019. http://hdl.handle.net/2433/242519.
Texto completoDuvvuri, Krishnaja. "Transition Metal Catalyzed Enantioselective Hydroboration and Hydrovinylation of Alkenes". The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1524049349604356.
Texto completoLibros sobre el tema "Transition-metal catalyzed organic transformations"
Kazmaier, Uli, ed. Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-22749-3.
Texto completoKazmaier, Uli. Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2012.
Buscar texto completoYamaguchi, Ryohei. Ligand platforms in homogenous catalytic reactions with metals: Practice and applications for green organic transformations. Hoboken, New Jersey: Wiley, 2015.
Buscar texto completoWang, Jianbo, Chi‐Ming Che y Michael P. Doyle, eds. Transition Metal‐Catalyzed Carbene Transformations. Wiley, 2022. http://dx.doi.org/10.1002/9783527829170.
Texto completoWang, Jianbo. Transition Metal-Catalyzed Carbene Transformations. Wiley & Sons, Limited, John, 2022.
Buscar texto completoWang, Jianbo. Transition Metal-Catalyzed Carbene Transformations. Wiley & Sons, Incorporated, John, 2022.
Buscar texto completoWang, Jianbo. Transition Metal-Catalyzed Carbene Transformations. Wiley & Sons, Limited, John, 2021.
Buscar texto completoWang, Jianbo. Transition Metal-Catalyzed Carbene Transformations. Wiley & Sons, Incorporated, John, 2022.
Buscar texto completoWu, Xiao-Feng. Transition Metal-Catalyzed Indole Synthesis: Transition Metal-Catalyzed Heterocycle Synthesis Series. Elsevier Science & Technology Books, 2017.
Buscar texto completoToste, F. Dean y A. Stephen K. Hashmi. Modern Gold Catalyzed Synthesis. Wiley-VCH Verlag GmbH, 2012.
Buscar texto completoCapítulos de libros sobre el tema "Transition-metal catalyzed organic transformations"
Guillena, Gabriela y Diego J. Ramón. "Metal-Catalyzed Methodologies". En Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis, 307–38. Hoboken, NJ, USA: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119006220.ch11.
Texto completoSandoval, Christian A., Ryoji Noyori, Qi-Lin Zhou, Andreas Pfaltz, Xue-Long Hou y Hisashi Yamamoto. "An Overview of Recent Developments in Metal-Catalyzed Asymmetric Transformations". En Organic Chemistry - Breakthroughs and Perspectives, 335–66. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527664801.ch9.
Texto completoPraneeth, V. K. K. y Thomas R. Ward. "Metal-Catalyzed Organic Transformations Inside a Protein Scaffold using Artificial Metalloenzymes". En Coordination Chemistry in Protein Cages, 203–19. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118571811.ch8.
Texto completoShao, Lixiong, Jianmei Lu y Min Shi. "Transition Metal-Catalyzed Transformations of VDCPs". En SpringerBriefs in Molecular Science, 41–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-27573-9_3.
Texto completoRusso, Francesco, Luke R. Odell, Kristofer Olofsson, Peter Nilsson y Mats Larhed. "Microwave-Heated Transition Metal-Catalyzed Coupling Reactions". En Microwaves in Organic Synthesis, 607–71. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch15.
Texto completoGrossman, Robert B. "Transition-Metal-Catalyzed and -Mediated Reactions". En The Art of Writing Reasonable Organic Reaction Mechanisms, 256–309. New York, NY: Springer New York, 1999. http://dx.doi.org/10.1007/978-1-4757-3030-2_6.
Texto completoGrossman, Robert B. "Transition-Metal-Mediated and -Catalyzed Reactions". En The Art of Writing Reasonable Organic Reaction Mechanisms, 341–414. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-28733-7_6.
Texto completoGrossman, Robert B. "Transition-Metal-Catalyzed and -Mediated Reactions". En The Art of Writing Reasonable Organic Reaction Mechanisms, 270–333. New York, NY: Springer New York, 2003. http://dx.doi.org/10.1007/0-387-21545-x_6.
Texto completoMoberg, Christina. "Molybdenum-Catalyzed and Tungsten-Catalyzed Enantioselective Allylic Substitutions". En Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis, 209–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/3418_2011_11.
Texto completoBrandsma, L., H. D. Verkruijsse y S. F. Vasilevsky. "Copper-Catalyzed Aminoalkylation of Acetylenes". En Application of Transition Metal Catalysts in Organic Synthesis, 61–67. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-60328-0_4.
Texto completoActas de conferencias sobre el tema "Transition-metal catalyzed organic transformations"
Huszár, Bianka, Zoltán Mucsi y György Keglevich. "Transition Metal-Catalyzed, “Ligand Free” P–C Coupling Reactions under MW Conditions". En International Electronic Conference on Synthetic Organic Chemistry. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13647.
Texto completoPadwa, Albert. "Synthesis of Polycyclic Ring Systems Using Transition Metal Catalyzed Cyclizations of Diazo Alkynyl Ketones". En The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01782.
Texto completoInformes sobre el tema "Transition-metal catalyzed organic transformations"
Transition metal catalyzed transformations of unsaturated molecules. Office of Scientific and Technical Information (OSTI), enero de 1989. http://dx.doi.org/10.2172/5417738.
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