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Статті в журналах з теми "Sulfoximine Directed C-H Activation"
Li, Yang, and Lin Dong. "Rhodium-catalyzed benzoisothiazole synthesis by tandem annulation reactions of sulfoximines and activated olefins." Organic & Biomolecular Chemistry 15, no. 47 (2017): 9983–86. http://dx.doi.org/10.1039/c7ob02586f.
Повний текст джерелаYadav, M. Ramu, Raja K. Rit, and Akhila K. Sahoo. "Sulfoximine Directed Intermolecular o-C–H Amidation of Arenes with Sulfonyl Azides." Organic Letters 15, no. 7 (March 11, 2013): 1638–41. http://dx.doi.org/10.1021/ol400411v.
Повний текст джерелаGabriele, Bartolo. "ChemInform Abstract: Geometrically Directed C-H Activation." ChemInform 44, no. 43 (October 7, 2013): no. http://dx.doi.org/10.1002/chin.201343224.
Повний текст джерелаYadav, M. Ramu, Raja K. Rit, and Akhila K. Sahoo. "ChemInform Abstract: Sulfoximine Directed Intermolecular o-C-H Amidation of Arenes with Sulfonyl Azides." ChemInform 44, no. 31 (July 11, 2013): no. http://dx.doi.org/10.1002/chin.201331076.
Повний текст джерелаSunnam, Sunil Kumar, and Jitendra D. Belani. "Aryne Multicomponent Reactions by Directed C−H Activation." Chemistry – A European Journal 27, no. 34 (May 26, 2021): 8846–50. http://dx.doi.org/10.1002/chem.202100205.
Повний текст джерелаTóth, Balázs L., Anna Monory, Orsolya Egyed, Attila Domján, Attila Bényei, Bálint Szathury, Zoltán Novák, and András Stirling. "The ortho effect in directed C–H activation." Chemical Science 12, no. 14 (2021): 5152–63. http://dx.doi.org/10.1039/d1sc00642h.
Повний текст джерелаSun, Qiao, and Naohiko Yoshikai. "Cobalt-catalyzed C(sp2)–H/C(sp3)–H coupling via directed C–H activation and 1,5-hydrogen atom transfer." Organic Chemistry Frontiers 5, no. 4 (2018): 582–85. http://dx.doi.org/10.1039/c7qo00906b.
Повний текст джерелаLiu, Yunyun, and Baoli Zhao. "Step-Economical C–H Activation Reactions Directed by In Situ Amidation." Synthesis 52, no. 21 (May 18, 2020): 3211–18. http://dx.doi.org/10.1055/s-0040-1707124.
Повний текст джерелаKondalarao, Koneti, Somratan Sau, and Akhila K. Sahoo. "Sulfoximine Assisted C–H Activation and Annulation via Vinylene Transfer: Access to Unsubstituted Benzothiazines." Molecules 28, no. 13 (June 27, 2023): 5014. http://dx.doi.org/10.3390/molecules28135014.
Повний текст джерелаJun, C. H., and J. H. Lee. "Application of C-H and C-C bond activation in organic synthesis." Pure and Applied Chemistry 76, no. 3 (January 1, 2004): 577–87. http://dx.doi.org/10.1351/pac200476030577.
Повний текст джерелаДисертації з теми "Sulfoximine Directed C-H Activation"
Guo, 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.
Wan, Yung-Chih, and 萬勇志. "Pd-catalyzed synthesis of fluorenones via nitrile directed C-H bond activation." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/68362267711970399165.
Повний текст джерела淡江大學
化學學系碩士班
101
We are successfully in developing a composite system of [Pd]/[Ag]/TFA to catalyze cascade reactions of nitrile directed remote C–H bond activation with insertion of nitrile (part 1), meanwhile, as we change the starting materials from Biphenyl-2-carbonitriles to Benzonitriles and Iodobenzenes (part 2) , the desired products could also be obtained by changing the species of the silver ions donor and it’s stoichiometric amount, through the using of this composite system, variously poly-substituted fluorenones were afforded in moderate to good yields with tolerance of a wide variety of substrates. In third part, 2''-Bromo-[1,1''-biphenyl]-2-carbonitriles were as starting materials which were reacted with Grignard reagent and catalyzed by copper to synthesize phenanthridines in one-pot, further studies to explore the tolerance of the different substrates are currently underway.
ZHAO, YIGANG. "Reduction of Tertiary Benzamides to Benzaldehydes by an in situ-Generated Schwartz Reagent (Cp2Zr(H)Cl); Formal Synthesis of Lysergic Acid 2. Ru-Catalyzed Amide-Directed Aryl C-H, C-N and C-O Bond Functionalizations: C-B Formation, C-C Suzuki Cross Coupling and Hydrodemethoxylation." Thesis, 2010. http://hdl.handle.net/1974/6671.
Повний текст джерелаThesis (Ph.D, Chemistry) -- Queen's University, 2010-12-21 11:12:35.564
Chen, Yu-Wen, and 陳俞汶. "Part I: Aryl Coupling Directed by C-H Activation Using Organocatalyst;Part II: Tuning Bis-Quinoline-Oligopyrrole Amide Conjugate." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/88122480235096968292.
Повний текст джерела國立中山大學
化學系研究所
101
Part I: The substructure of biaryl is an important motif in many pharmaceutically relevant and biologically active compounds. As a result, for over a century, organic chemists have sought to develop new and more efficient aryl-aryl bond forming methods. However, using of transition metals to synthetic drugs is limited by residuals of metal impurities and the financial cost of the metal catalyst. Therefore the purpose of our experiment is to find an organocatalytic method for constructing biaryls through aromatic C-H activation. Synthetic phenanthroline derivatives were treated as organocatalyst for different aromatic and heterocyclic ring coupling reactions. Part II: Inhibition of telomerase activity through inducing or stabilization of G-quadruplex DNA structures of human telomere was capable to achieve the anti-cancer effect. The first improvement is the synthesis of Bis-quinoline in the past laboratory ways to reduce the number of steps. Synthetic Bis-quinoline oligopyrrole compounds were found to interact with G-quadruplex DNA slightly and they were assumed to be limited by the rigid structure. In this study, we are attempting to introduce glycine as the connection bridge between bis-quinoline and oligopyrrole. Therefore the softer structures are expecting to better fit into the G-quadruplex DNA secondary structure.
Частини книг з теми "Sulfoximine Directed C-H Activation"
Shang, Rui. "Recent Developments of Iron-Catalyzed Directed C–H Activation/C–C Bond Formation Reactions." In Springer Theses, 161–74. Singapore: Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-3193-9_9.
Повний текст джерелаDavies, H. M. L., and D. Morton. "Heteroatom-Directed C—H Functionalization." In Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00354.
Повний текст джерелаDavies, H. M. L., and D. Morton. "Directed sp C—H Bond Insertion." In Stereoselective Pericyclic Reactions, Cross Coupling, and C—H and C—X Activation, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-203-00337.
Повний текст джерелаChatani, N. "1.14 Nickel-Catalyzed Directed C—H Functionalization." In Base-Metal Catalysis 1. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-238-00266.
Повний текст джерелаThrimurtulu, Neetipalli, Aniruddha Dey, Debabrata Maiti, and Chandra M. R. Volla. "Recent Developments in Palladium-Catalyzed Natural Product Synthesis via C H Activation." In Strategies for Palladium-Catalyzed Non-Directed and Directed C-H Bond Functionalization, 453–70. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-805254-9.00012-8.
Повний текст джерелаBanerjee, S., and L. Ilies. "2.8 Iron-Catalyzed C—H Functionalization." In Base-Metal Catalysis 2. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-239-00143.
Повний текст джерелаTaber, Douglass F. "C-H Functionalization: The Chen Synthesis of Celogentin C." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0019.
Повний текст джерелаK. Patel, Bhisma, and Amitava Rakshit. "Access to N-Heterocyclic Molecules via Ru(II)-Catalyzed Oxidative Alkyne Annulation Reactions." In Ruthenium - an Element Loved by Researchers [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.95987.
Повний текст джерелаТези доповідей конференцій з теми "Sulfoximine Directed C-H Activation"
Meusburger, S., R. Beckmann, J. Wojta, and B. R. Binder. "RELATION OP FIBRIN STIMULATION OF tPA MEDIATED PLASMINOGEN ACTIVATION AND FIBRIN BINDING TOWARDS FIBRONEKTIN AS REVEALED BY A MONOCLONAL ANTIBODY (MAB) AGAINST FCB-2 FIBRINOGEN FRAGMENTS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644403.
Повний текст джерелаGimbrone, M. A., M. P. Bevilacqua, and M. E. Wheeler. "ENDOTHELIAL-DEPENDENT MECHANISMS OF LEUKOCYTE ADHESION: ROLE OF MONOKINES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643983.
Повний текст джерелаЗвіти організацій з теми "Sulfoximine Directed C-H Activation"
Rafaeli, Ada, and Russell Jurenka. Molecular Characterization of PBAN G-protein Coupled Receptors in Moth Pest Species: Design of Antagonists. United States Department of Agriculture, December 2012. http://dx.doi.org/10.32747/2012.7593390.bard.
Повний текст джерела