Добірка наукової літератури з теми "Transition-metal catalyzed organic transformations"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Transition-metal catalyzed organic transformations".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Transition-metal catalyzed organic transformations"
Mhaske, Santosh, and Ranjeet Dhokale. "Transition-Metal-Catalyzed Reactions Involving Arynes." Synthesis 50, no. 01 (November 22, 2017): 1–16. http://dx.doi.org/10.1055/s-0036-1589517.
Повний текст джерелаKuninobu, Yoichiro. "Transition Metal-Catalyzed Highly Efficient and Novel Transformations." Journal of Synthetic Organic Chemistry, Japan 71, no. 5 (2013): 425–32. http://dx.doi.org/10.5059/yukigoseikyokaishi.71.425.
Повний текст джерелаTakacs, J. M., S. C. Boito, and Y. C. Myoung. "Recent Applications of Catalytic Metal-Mediated Carbocyclizations in Asymmetric Synthesis." Current Organic Chemistry 2, no. 3 (May 1998): 233–54. http://dx.doi.org/10.2174/1385272802666220128192732.
Повний текст джерелаYuan, Jia, Ying Zhang, Hong Yu, Cuiying Wang, Sixuan Meng, Jian Chen, Guang-Ao Yu, and Chi-Ming Che. "Transition metal complexes with functionalized indenyl phosphine ligands: structures and catalytic properties." Organic & Biomolecular Chemistry 20, no. 3 (2022): 485–97. http://dx.doi.org/10.1039/d1ob01884a.
Повний текст джерелаZuo, Linhong, Teng Liu, Xiaowei Chang, and Wusheng Guo. "An Update of Transition Metal-Catalyzed Decarboxylative Transformations of Cyclic Carbonates and Carbamates." Molecules 24, no. 21 (October 31, 2019): 3930. http://dx.doi.org/10.3390/molecules24213930.
Повний текст джерелаSala, Roberto, Camilla Loro, Francesca Foschi, and Gianluigi Broggini. "Transition Metal Catalyzed Azidation Reactions." Catalysts 10, no. 10 (October 12, 2020): 1173. http://dx.doi.org/10.3390/catal10101173.
Повний текст джерелаXu, Qing, Changqiu Zhao, Yongbo Zhou, Shuangfeng Yin, and Libiao Han. "Transition Metal-Catalyzed Transformations of P(O)—H Bonds." Chinese Journal of Organic Chemistry 32, no. 10 (2012): 1761. http://dx.doi.org/10.6023/cjoc201207024.
Повний текст джерелаDella Ca’, Nicola. "Palladium-Catalyzed Reactions." Catalysts 11, no. 5 (April 30, 2021): 588. http://dx.doi.org/10.3390/catal11050588.
Повний текст джерелаLandelle, Grégory, Armen Panossian, Sergiy Pazenok, Jean-Pierre Vors, and Frédéric R. Leroux. "Recent advances in transition metal-catalyzed Csp2-monofluoro-, difluoro-, perfluoromethylation and trifluoromethylthiolation." Beilstein Journal of Organic Chemistry 9 (November 15, 2013): 2476–536. http://dx.doi.org/10.3762/bjoc.9.287.
Повний текст джерелаMarset, Xavier, and Gabriela Guillena. "Deep Eutectic Solvents as à-la-Carte Medium for Transition-Metal-Catalyzed Organic Processes." Molecules 27, no. 23 (December 2, 2022): 8445. http://dx.doi.org/10.3390/molecules27238445.
Повний текст джерелаДисертації з теми "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.
Повний текст джерелаGanguly, 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.
Повний текст джерелаGandolfo, Eugenio. "Light-driven Metal-catalyzed Asymmetric Transformations." Doctoral thesis, Universitat Rovira i Virgili, 2021. http://hdl.handle.net/10803/672439.
Повний текст джерелаResumen 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.
Повний текст джерелаTan, 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.
Повний текст джерелаSong, Xuejing. "Studies of transition metal catalyzed propylene polymerization." Thesis, University of Oxford, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308611.
Повний текст джерелаZweni, Pumza P. "Dendrimer-transition metal catalyzed oxidation and reduction reactions." Thesis, University of Ottawa (Canada), 2005. http://hdl.handle.net/10393/10529.
Повний текст джерелаTrono, 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.
Повний текст джерелаTatsumi, Kenta. "Transition Metal-Catalyzed Novel Transformations of Acid Chlorides and Acid Anhydrides." Kyoto University, 2019. http://hdl.handle.net/2433/242519.
Повний текст джерелаDuvvuri, Krishnaja. "Transition Metal Catalyzed Enantioselective Hydroboration and Hydrovinylation of Alkenes." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1524049349604356.
Повний текст джерелаКниги з теми "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.
Повний текст джерелаKazmaier, Uli. Transition Metal Catalyzed Enantioselective Allylic Substitution in Organic Synthesis. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2012.
Знайти повний текст джерелаYamaguchi, Ryohei. Ligand platforms in homogenous catalytic reactions with metals: Practice and applications for green organic transformations. Hoboken, New Jersey: Wiley, 2015.
Знайти повний текст джерелаWang, Jianbo, Chi‐Ming Che, and Michael P. Doyle, eds. Transition Metal‐Catalyzed Carbene Transformations. Wiley, 2022. http://dx.doi.org/10.1002/9783527829170.
Повний текст джерелаWang, Jianbo. Transition Metal-Catalyzed Carbene Transformations. Wiley & Sons, Limited, John, 2022.
Знайти повний текст джерелаWang, Jianbo. Transition Metal-Catalyzed Carbene Transformations. Wiley & Sons, Incorporated, John, 2022.
Знайти повний текст джерелаWang, Jianbo. Transition Metal-Catalyzed Carbene Transformations. Wiley & Sons, Limited, John, 2021.
Знайти повний текст джерелаWang, Jianbo. Transition Metal-Catalyzed Carbene Transformations. Wiley & Sons, Incorporated, John, 2022.
Знайти повний текст джерелаWu, Xiao-Feng. Transition Metal-Catalyzed Indole Synthesis: Transition Metal-Catalyzed Heterocycle Synthesis Series. Elsevier Science & Technology Books, 2017.
Знайти повний текст джерелаToste, F. Dean, and A. Stephen K. Hashmi. Modern Gold Catalyzed Synthesis. Wiley-VCH Verlag GmbH, 2012.
Знайти повний текст джерелаЧастини книг з теми "Transition-metal catalyzed organic transformations"
Guillena, Gabriela, and Diego J. Ramón. "Metal-Catalyzed Methodologies." In 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.
Повний текст джерелаSandoval, Christian A., Ryoji Noyori, Qi-Lin Zhou, Andreas Pfaltz, Xue-Long Hou, and Hisashi Yamamoto. "An Overview of Recent Developments in Metal-Catalyzed Asymmetric Transformations." In Organic Chemistry - Breakthroughs and Perspectives, 335–66. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527664801.ch9.
Повний текст джерелаPraneeth, V. K. K., and Thomas R. Ward. "Metal-Catalyzed Organic Transformations Inside a Protein Scaffold using Artificial Metalloenzymes." In Coordination Chemistry in Protein Cages, 203–19. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118571811.ch8.
Повний текст джерелаShao, Lixiong, Jianmei Lu, and Min Shi. "Transition Metal-Catalyzed Transformations of VDCPs." In SpringerBriefs in Molecular Science, 41–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-27573-9_3.
Повний текст джерелаRusso, Francesco, Luke R. Odell, Kristofer Olofsson, Peter Nilsson, and Mats Larhed. "Microwave-Heated Transition Metal-Catalyzed Coupling Reactions." In Microwaves in Organic Synthesis, 607–71. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527651313.ch15.
Повний текст джерелаGrossman, Robert B. "Transition-Metal-Catalyzed and -Mediated Reactions." In 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.
Повний текст джерелаGrossman, Robert B. "Transition-Metal-Mediated and -Catalyzed Reactions." In 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.
Повний текст джерелаGrossman, Robert B. "Transition-Metal-Catalyzed and -Mediated Reactions." In 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.
Повний текст джерелаMoberg, Christina. "Molybdenum-Catalyzed and Tungsten-Catalyzed Enantioselective Allylic Substitutions." In 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.
Повний текст джерелаBrandsma, L., H. D. Verkruijsse, and S. F. Vasilevsky. "Copper-Catalyzed Aminoalkylation of Acetylenes." In 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.
Повний текст джерелаТези доповідей конференцій з теми "Transition-metal catalyzed organic transformations"
Huszár, Bianka, Zoltán Mucsi, and György Keglevich. "Transition Metal-Catalyzed, “Ligand Free” P–C Coupling Reactions under MW Conditions." In International Electronic Conference on Synthetic Organic Chemistry. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13647.
Повний текст джерелаPadwa, Albert. "Synthesis of Polycyclic Ring Systems Using Transition Metal Catalyzed Cyclizations of Diazo Alkynyl Ketones." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01782.
Повний текст джерелаЗвіти організацій з теми "Transition-metal catalyzed organic transformations"
Transition metal catalyzed transformations of unsaturated molecules. Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/5417738.
Повний текст джерела