Добірка наукової літератури з теми "C–H Bond - Maleimides"
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Статті в журналах з теми "C–H Bond - Maleimides"
He, Qiyuan, Yusuke Ano, and Naoto Chatani. "The Pd-catalyzed C–H alkylation of ortho-methyl-substituted aromatic amides with maleimide occurs preferentially at the ortho-methyl C–H bond over the ortho-C–H bond." Chemical Communications 55, no. 67 (2019): 9983–86. http://dx.doi.org/10.1039/c9cc05321b.
Повний текст джерелаZhao, Sheng-Yin, Hong-Ru Tan, Lun Wang, Jia-Nan Zhu, and Zhen-Hua Yang. "Iodine-Promoted C(sp 2)–H Thiolation of Maleimides with Dimethyl Sulfoxide and Thiols." Synthesis 50, no. 20 (July 30, 2018): 4113–23. http://dx.doi.org/10.1055/s-0037-1609585.
Повний текст джерелаPan, Changduo, Yun Wang, Chao Wu, and Jin-Tao Yu. "Rhodium-catalyzed C7-alkylation of indolines with maleimides." Organic & Biomolecular Chemistry 16, no. 5 (2018): 693–97. http://dx.doi.org/10.1039/c7ob03039h.
Повний текст джерелаJeganmohan, Masilamani, Meledath Sudhakaran Keerthana, and Ramasamy Manoharan. "Cobalt(III)-Catalyzed Redox-Neutral Coupling of Acrylamides with Activated Alkenes via C–H Bond Activation." Synthesis 52, no. 11 (March 30, 2020): 1625–33. http://dx.doi.org/10.1055/s-0039-1690866.
Повний текст джерелаSun, Meng, Xiang-Xiang Chen, Jiang-Tao Ren, Jing-Lei Xu, Hu Xie, Wei Sun, and Ya-Min Li. "Cobalt(III)-Catalyzed 1,4-Addition of C(sp3)–H Bonds to Maleimides." Synlett 29, no. 12 (May 29, 2018): 1601–6. http://dx.doi.org/10.1055/s-0037-1609847.
Повний текст джерелаBettadapur, Kiran R., Veeranjaneyulu Lanke, and Kandikere Ramaiah Prabhu. "A deciduous directing group approach for the addition of aryl and vinyl nucleophiles to maleimides." Chemical Communications 53, no. 46 (2017): 6251–54. http://dx.doi.org/10.1039/c7cc02392h.
Повний текст джерелаZhao, Sheng-Yin, Zhen-Hua Yang, Jia-Nan Zhu, Ze-Hui Jin, and Jian Zheng. "Copper-Catalyzed Intermolecular Thioamination of Maleimides with Thiols and Formamides: A One-Step Construction of 3-Amino-4-thiomaleimides Using Formamides as Nitrogen Sources." Synthesis 50, no. 23 (August 7, 2018): 4627–36. http://dx.doi.org/10.1055/s-0037-1610536.
Повний текст джерелаChen, Xiangxiang, Jiangtao Ren, Hu Xie, Wei Sun, Meng Sun, and Biao Wu. "Cobalt(iii)-catalyzed 1,4-addition of C–H bonds of oximes to maleimides." Organic Chemistry Frontiers 5, no. 2 (2018): 184–88. http://dx.doi.org/10.1039/c7qo00687j.
Повний текст джерелаMangialetto, Jessica, Kiano Gorissen, Lise Vermeersch, Bruno Van Mele, Niko Van den Brande, and Freija De Vleeschouwer. "Hydrogen-Bond-Assisted Diels–Alder Kinetics or Self-Healing in Reversible Polymer Networks? A Combined Experimental and Theoretical Study." Molecules 27, no. 6 (March 17, 2022): 1961. http://dx.doi.org/10.3390/molecules27061961.
Повний текст джерелаMuniraj, Nachimuthu, and Kandikere Ramaiah Prabhu. "Cobalt(III)-Catalyzed C–H Activation: Azo Directed Selective 1,4-Addition of Ortho C–H Bond to Maleimides." Journal of Organic Chemistry 82, no. 13 (June 19, 2017): 6913–21. http://dx.doi.org/10.1021/acs.joc.7b01094.
Повний текст джерелаДисертації з теми "C–H Bond - Maleimides"
Torkelson, Jeffrey Robert. "C-H bond activation and C-C bond formation at adjacent metals." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/NQ34848.pdf.
Повний текст джерелаGuo, Xiangyu. "Ruthenium-catalyzed C-C bond formation via functional-group directed C-H bond activation." Thesis, McGill University, 2012. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=110570.
Повний текст джерелаRésuméRuthenium-Catalyzed C-C Bond Formation via Functional-Group Directed C-H Bond ActivationXiangyu GuoSuperviseur: Prof. Chao-Jun LiUniversité McGillCette thèse est le résultat de la recherche sur la formation de liaisons carbone-carbone (C-C), catalysé par le ruthénium. La première partie de cette thèse expose les résultats sur la formation de liaison carbone-carbone (C-C) par la réaction de couplage oxydant par déshydrogénation. La synthèse de composés biaryl par l'utilisation d'un catalyseur de ruthénium a permis la dimérisation des dérivés de la 2-phénylpyridine en présence de chlorure de fer (III) comme oxydant terminal. En outre, l'oxydative cross-coupling entre arènes et cycloalcanes, a montrer une notable, para-sélectivité. La seconde partie de cette thèse, décrit les résultats obtenue sur la réaction d'oléfination decarbonylative entre un aldéhyde et un alcyne vrai, catalyser par le ruthénium. En partant d'aldéhydes aromatiques ou aliphatiques et par l'utilisation de deux systèmes catalytiques, la synthèse chemioselective de double liaison C=C conjuguée ou isolée ont pu être réalisé. Cette réaction fournit ainsi, une intéressante alternative à la synthèse de doubles liaisons C=C par la directe addition de liaison C-H sur une triple liaison.
Laren, Martijn Wouter van. "Palladium-catalyzed C-H and C-N bond formation." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2004. http://dare.uva.nl/document/75422.
Повний текст джерелаVastine, Benjamin Alan. "Understanding mechanisms for C-H bond activation." [College Station, Tex. : Texas A&M University, 2008. http://hdl.handle.net/1969.1/ETD-TAMU-2679.
Повний текст джерелаWiley, Jack Scott. "C-H bond activation in iridium complexes /." Thesis, Connect to this title online; UW restricted, 1999. http://hdl.handle.net/1773/8510.
Повний текст джерелаTruscott, Fiona Rosemary. "Transition metal catalysed C-C bond formation via C-H functionalisation." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:6a1ef296-8d63-470d-96bd-3e01a887c81f.
Повний текст джерелаCatino, Arthur John. "Oxidative C-H and C-C bond functionalization catalyzed by dirhodium caprolactamate." College Park, Md. : University of Maryland, 2006. http://hdl.handle.net/1903/4188.
Повний текст джерелаThesis research directed by: Chemistry. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.
Gao, Longhui. "C-H bond activation catalyzed by Ruthenium nanoparticles." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS348/document.
Повний текст джерелаDeuterated and tritiated compounds are widely used in numerous applications in chemistry, biology and material science. In the drug discovery and development process, ADME studies require quick access to labelled molecules, otherwise the drug development costs and timeline are significantly impacted. The rapid development of metabolomics has also increased the need for isotopically labelled compounds. In particular, deuterated molecules are used as internal standards for quantitative LC-MS/MS analysis of metabolites in biological fluids and tissues. In this context, a general method allowing the deuterium and tritium labelling of bioactive thioethers using a HIE reaction is described in the first chapter. From a fundamental point of view, this transformation is the first example of (Csp³)-H activation directed by a sulfur atom. In terms of application, this new reaction has been proved to be useful for the preparation of deuterated LC-MS/MS reference materials and tritiated pharmaceuticals owning high specific activity.In the second chapter of this manuscript, the development of a method allowing the cross-dehydrogenative homocoupling of 2-arylpyridines catalyzed by Ru/C is developed. Various substrates with different substituents were efficiently coupled to give the desired dimers in good yield. In terms of application, a series of pyridine-boron complexes derived from the phenyl pyridine dimers were also synthesized and their photophysical properties were studied.In the third chapter, a regioselective palladium catalyzed intramolecular arylation reaction allowing the synthesis of pyridine containing polycyclic compounds is described
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.
Повний текст джерелаLocati, Abel Jean Serge. "Computational study of c-h bond cleavage and c-c bond formation processes catalyzed by transition metal complexes." Doctoral thesis, Universitat Rovira i Virgili, 2012. http://hdl.handle.net/10803/79120.
Повний текст джерелаThe first part of the thesis is mainly devoted to the mechanism of a C-H activation reaction by a niobium complex. The mechanism of C-H bond activation of benzene by the TpMe2NbCH3-(c-C3H5)-(MeCCMe) complex was rationalized. The key intermediate is an unusual 2-cyclopropene complex. We rationalized the selectivities obtained for the activation of several alkylaromatics by the 2-cyclopropene niobium complex. The intriguing role of the alkyne ligand of the same complex, and its possible role in the migration processes, was investigated. In the second part of the thesis, we focused on the silicon based cross-coupling. The results suggest than the transmetalation is easier after phosphine dissociation, and in presence of the bromide ligand on the palladium. The beneficial effect of dibenzylideneacetone on the coupling was clarified.
Книги з теми "C–H Bond - Maleimides"
Ribas, Xavi, ed. C-H and C-X Bond Functionalization. Cambridge: Royal Society of Chemistry, 2013. http://dx.doi.org/10.1039/9781849737166.
Повний текст джерелаXie, Jin, and Chengjian Zhu. Sustainable C(sp3)-H Bond Functionalization. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49496-7.
Повний текст джерелаDixneuf, Pierre H., and Henri Doucet, eds. C-H Bond Activation and Catalytic Functionalization II. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29319-6.
Повний текст джерелаDixneuf, Pierre H., and Henri Doucet, eds. C-H Bond Activation and Catalytic Functionalization I. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-24630-7.
Повний текст джерелаMatsumoto, Arimasa. Iron-Catalyzed Synthesis of Fused Aromatic Compounds via C–H Bond Activation. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54928-4.
Повний текст джерелаMaiti, Debabrata, and Srimanta Guin, eds. Remote CH Bond Functionalizations. Wiley, 2021. http://dx.doi.org/10.1002/9783527824137.
Повний текст джерелаXie, Jin, and Chengjian Zhu. Sustainable C(sp3)-H Bond Functionalization. Springer, 2016.
Знайти повний текст джерелаXie, Jin, and Chengjian Zhu. Sustainable C(sp3)-H Bond Functionalization. Springer London, Limited, 2016.
Знайти повний текст джерелаLukašēvics, Tomass. Kobalta katalizēta C‒H saites funkcionalizēšana/Cobalt Catalyzed C‒H Bond Functionalization. RTU Press, 2022. http://dx.doi.org/10.7250/9789934227806.
Повний текст джерелаC-H Bond Activation in Organic Synthesis. Taylor & Francis Group, 2015.
Знайти повний текст джерелаЧастини книг з теми "C–H Bond - Maleimides"
Satoh, Tetsuya, and Masahiro Miura. "C-H Bond Alkenylation." In Metal-Catalyzed Cross-Coupling Reactions and More, 1389–426. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527655588.ch18.
Повний текст джерелаOtake, Masayuki. "Energy Storage in C–C, H–H and C–H Bond." In Lecture Notes in Energy, 123–33. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-25400-5_8.
Повний текст джерелаBouffard, Jean, and Kenichiro Itami. "Rhodium-Catalyzed C–H Bond Arylation of Arenes." In C-H Activation, 231–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/128_2009_12.
Повний текст джерелаWasa, Masayuki, Kelvin S. L. Chan, and Jin-Quan Yu. "Asymmetric C-H Bond Functionalization." In Asymmetric Synthesis II, 267–72. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527652235.ch33.
Повний текст джерелаLiu, Guosheng, and Yichen Wu. "Palladium-Catalyzed Allylic C–H Bond Functionalization of Olefins." In C-H Activation, 195–209. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/128_2009_16.
Повний текст джерелаAckermann, Lutz, and Rubén Vicente. "Ruthenium-Catalyzed Direct Arylations Through C–H Bond Cleavages." In C-H Activation, 211–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/128_2009_9.
Повний текст джерелаLebel, Hélène. "Rhodium-Catalyzed CH Aminations." In Catalyzed Carbon-Heteroatom Bond Formation, 137–55. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch5.
Повний текст джерелаYou, Shu-Li, and Ji-Bao Xia. "Palladium-Catalyzed Aryl–Aryl Bond Formation Through Double C–H Activation." In C-H Activation, 165–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/128_2009_18.
Повний текст джерелаBeck, Elizabeth M., and Matthew J. Gaunt. "Pd-Catalyzed C–H Bond Functionalization on the Indole and Pyrrole Nucleus." In C-H Activation, 85–121. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/128_2009_15.
Повний текст джерелаIlies, Laurean, and Eiichi Nakamura. "Iron-Catalyzed C–H Bond Activation." In Topics in Organometallic Chemistry, 1–18. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_129.
Повний текст джерелаТези доповідей конференцій з теми "C–H Bond - Maleimides"
Ulin-Avila, Erick, and Akhilesh Kumar Mishra. "Graphene-based Photonic C-H bond activation." In Frontiers in Optics. Washington, D.C.: OSA, 2021. http://dx.doi.org/10.1364/fio.2021.jtu1a.55.
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 джерелаNyambo, Silver, Dong-Sheng Yang, and Yuchen Zhang. "PROBING SELECTIVE BOND ACTIVATION IN ALKYLAMINES: LANTHANUM-MEDIATED C-H AND N-H BOND ACTIVATION STUDIED BY MATI SPECTROSCOPY." In 73rd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.fb01.
Повний текст джерелаKim, Jong, and Dong-Sheng Yang. "YTTRIUM-ASSISTED C-H AND C-C BOND ACTIVATION OF ETHYLENE PROBED BY MASS-ANALYZED THRESHOLD IONIZATION SPECTROSCOPY." In 71st International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.ri06.
Повний текст джерелаLian, T., S. E. Bromberg, H. Yang, M. Asplund, R. G. Bergman, and C. B. Harris. "Femtosecond IR Studies of Alkane C-H Bond Activation by Organometallic Compounds." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.fe.27a.
Повний текст джерелаBaba, Masaaki, Umpei Nagashima, and Tsuneo Hirano. "AB INITIO CALCULATIONS ON ROTATIONAL CONSTANT AND AVERAGED C-H(D) BOND LENGTHS OF BENZENE." In 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.tj09.
Повний текст джерелаKim, Jong, and Dong-Sheng Yang. "SPECTROSCOPIC IDENTIFICATION OF Y(C4H6) ISOMERS FORMED BY YTTRIUM-MEDIATED C-H BOND ACTIVATION OF BUTENES." In 71st International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.mh09.
Повний текст джерелаSubramanian, Raghavendran, and Kazem Kazerounian. "Improved Molecular Model of a Peptide Unit for Proteins." In ASME 2006 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2006. http://dx.doi.org/10.1115/detc2006-99315.
Повний текст джерелаPint, Bruce A., Michael J. Lance, and J. Allen Haynes. "The Effect of Coating Composition and Geometry on TBC Lifetime." In ASME Turbo Expo 2017: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/gt2017-65103.
Повний текст джерелаJay, Raphael M., Ambar Banerjee, Torsten Leitner, Robert Stefanuik, Ru-Pan Wang, Jessica Harich, Emma Beale, et al. "From Femtosecond Excited-State and Dissociation Dynamics to Nanosecond Reaction Kinetics: Following C-H Bond Activation with X-rays." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/up.2022.tu1a.2.
Повний текст джерелаЗвіти організацій з теми "C–H Bond - Maleimides"
Lees, Alistair J. Photochemistry of Intermolecular C-H Bond Activation Reactions. Office of Scientific and Technical Information (OSTI), June 2000. http://dx.doi.org/10.2172/761218.
Повний текст джерелаAsplund, M. C. Time resolved infrared studies of C-H bond activation by organometallics. Office of Scientific and Technical Information (OSTI), June 1998. http://dx.doi.org/10.2172/290889.
Повний текст джерелаLees, A. J. [Photochemistry of intermolecular C-H bond activation reactions]. Progress report, [September 15, 1994--March 15, 1995]. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/35271.
Повний текст джерела