Добірка наукової літератури з теми "Catalytic C-H"
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Статті в журналах з теми "Catalytic C-H"
Hilinski, Michael, Shea Johnson, and Logan Combee. "Organocatalytic Atom-Transfer C(sp3)–H Oxidation." Synlett 29, no. 18 (June 27, 2018): 2331–36. http://dx.doi.org/10.1055/s-0037-1610432.
Повний текст джерелаZhang, Hua, and Li Wang. "Metal-Free Catalytic Aromatic C–H Borylation." Synlett 31, no. 19 (August 11, 2020): 1857–61. http://dx.doi.org/10.1055/s-0040-1707241.
Повний текст джерелаKakiuchi, Fumitoshi, and Shinji Murai. "Catalytic C−H/Olefin Coupling." Accounts of Chemical Research 35, no. 10 (October 2002): 826–34. http://dx.doi.org/10.1021/ar960318p.
Повний текст джерелаMurai, S., F. Kakiuchi, S. Sekine, Y. Tanaka, Asayuki Kamatani, M. Sonoda, and Naoto Chatani. "Catalytic C-H/olefin coupling." Pure and Applied Chemistry 66, no. 7 (January 1, 1994): 1527–34. http://dx.doi.org/10.1351/pac199466071527.
Повний текст джерелаBach, T., A. Nörder, P. Herrmann, and E. Herdtweck. "Diastereoselective Catalytic C-H Amination." Synfacts 2010, no. 10 (September 22, 2010): 1141. http://dx.doi.org/10.1055/s-0030-1258647.
Повний текст джерелаChen, Qing-An, Wei-Song Zhang, and Yan-Cheng Hu. "Isoprene: A Promising Coupling Partner in C–H Functionalizations." Synlett 31, no. 17 (July 2, 2020): 1649–55. http://dx.doi.org/10.1055/s-0040-1707172.
Повний текст джерелаNishii, Yuji, and Masahiro Miura. "Construction of Benzo-Fused Polycyclic Heteroaromatic Compounds through Palladium-Catalyzed Intramolecular C-H/C-H Biaryl Coupling." Catalysts 13, no. 1 (December 22, 2022): 12. http://dx.doi.org/10.3390/catal13010012.
Повний текст джерелаCollet, Florence, Camille Lescot, Chungen Liang, and Philippe Dauban. "Studies in catalytic C–H amination involving nitrene C–H insertion." Dalton Transactions 39, no. 43 (2010): 10401. http://dx.doi.org/10.1039/c0dt00283f.
Повний текст джерелаBedford, Robin B., Charlotte J. Mitchell, and Ruth L. Webster. "Solvent free catalytic C–H functionalisation." Chemical Communications 46, no. 18 (2010): 3095. http://dx.doi.org/10.1039/c003074k.
Повний текст джерелаYoung, Andrew J., and M. Christina White. "Catalytic Intermolecular Allylic CH Alkylation." Journal of the American Chemical Society 130, no. 43 (October 29, 2008): 14090–91. http://dx.doi.org/10.1021/ja806867p.
Повний текст джерелаДисертації з теми "Catalytic C-H"
Leitch, Jamie. "Site selective catalytic C-H functionalisation." Thesis, University of Bath, 2017. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767559.
Повний текст джерелаReynolds, William. "Sequential processes involving catalytic C-H functionalisation." Thesis, University of Bath, 2014. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.642028.
Повний текст джерелаPaterson, Andrew. "Selective catalytic C-H functionalisation for drug discovery." Thesis, University of Bath, 2017. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.720659.
Повний текст джерелаIngner, Fredric. "Preparation of carbazolyne precursors through catalytic C-H functionalization." Thesis, Uppsala universitet, Organisk kemi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-307497.
Повний текст джерелаGallardo, Donaire Juan. "Synthesis of phthalides and benzolactones via catalytic C-H functionalization/C-O bond-forming." Doctoral thesis, Universitat Rovira i Virgili, 2014. http://hdl.handle.net/10803/276960.
Повний текст джерелаThe main objective of this Thesis has been the activation of inert C-H bonds catalytically for the construction of C-O bonds. The fist project developed consisted on the activation of C(sp3)-H bonds for the direct synthesis of phthalides catalyzed by Pd, employing simple benzoic acids as starting materials. Continuing in the same research line, the second project described deals with the utilization of cheaper and easy to handle Cu salts as catalyst for the functionalization of C(sp2)-H bonds towards the formation of C-O bonds for the synthesis of benzolactones. Finally, the last project discovered handles a metal-free C-H functionalization approach for the synthesis of benzolactones by using simple iodoarenes as catalyst, thus
Stateman, Leah Marie. "Catalytic Strategies for Remote C-H Functionalization of Alcohols and Amines." The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1587554146078308.
Повний текст джерелаWang, Chang-Sheng. "Selective catalytic C(sp²)–H and C(sp³)–H bond functionalizations for the synthesis of phosphorus and nitrogen containing molecules." Thesis, Rennes 1, 2018. http://www.theses.fr/2018REN1S106/document.
Повний текст джерелаIn the first chapter, we have developed an efficient approach for the fast modification of arylphosphine oxides using ruthenium(II)-catalyzed C–H bond functionalization with alkenes. Interestingly, we have found that the selectivity of the reaction, namely alkylation versus alkenylation, is depending on the reaction pH. The reduction of the phosphine oxide allows the formation of aryl phosphines bearing a flexible pendent carboxylate. In the second objective, a copper-catalyzed oxidative C(sp3)–H/N–H coupling of NH-heterocycles with affordable (cyclo)alkanes was developed. This protocol involved C(sp3)–N bond formation via a radical pathway generated by a homolytic cleavage of di-tert-butyl peroxide and trapping of the radical(s) by copper catalyst.In a third part, benzylic C(sp3)–H acyloxylation of 2-alkylpyridine, 2-alkylpyrazine and 2-alkylthiazole compounds was achieved using simple aldehydes via a copper-catalyzed tandem reaction, involving oxidative esterification followed by O-atom transfer. Finally, pyridin-2-ylmethyl tosylate derivatives are obtained in high yields from 2-alkylpyridine N-oxides via a [3,3]-sigmatropic rearrangement of the adduct between 2-alkylpridine N-oxides with benzenesolfonyl chlorides. Moreover, alkylnitrones also underwant [3,3]-sigmatropic rearrangement to give α-tosylated ketones after hydrolysis
Gerdes, Gerd. "Catalytic C-H activation of benzene by plantinum(II) : a mechanistic study /." Zürich, 2004. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=15631.
Повний текст джерелаSankey, Rosalind Fay. "Beyond C-H activation : the preparation of novel heterocycles using catalytic dearomatisation." Thesis, University of Bristol, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559388.
Повний текст джерелаKhan, Imtiaz. "Enolate-directed catalytic C-H functionalization of 2-aryl-1,3-dicarbonyl compounds." Thesis, University of Nottingham, 2015. http://eprints.nottingham.ac.uk/30261/.
Повний текст джерелаКниги з теми "Catalytic C-H"
Dixneuf, 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 джерелаJacques, Teresa. I : Catalytic Direct C-H Arylation of Pyrazoles. II: Toward Modulation of Neuroplasticity with Small Molecules. [New York, N.Y.?]: [publisher not identified], 2013.
Знайти повний текст джерелаPérez, Pedro J., ed. Alkane C-H Activation by Single-Site Metal Catalysis. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-3698-8.
Повний текст джерелаBergeld, Johan. Thermo- and photostimulated reactions of H₂O, O₂, and CO on Pt(111) and C(0001) surfaces. Göteborg: Göteborg University, Department of Physics, 2007.
Знайти повний текст джерелаCatalytic Transformations Via C-H Activation 1. Thieme Verlag, George, 2016.
Знайти повний текст джерелаDixneuf, Pierre H., and Henri Doucet. C-H Bond Activation and Catalytic Functionalization II. Springer London, Limited, 2016.
Знайти повний текст джерелаDixneuf, Pierre H., and Henri Doucet. C-H Bond Activation and Catalytic Functionalization II. Springer, 2016.
Знайти повний текст джерелаDixneuf, Pierre H., and Henri Doucet. C-H Bond Activation and Catalytic Functionalization I. Springer, 2018.
Знайти повний текст джерелаDixneuf, Pierre H., and Henri Doucet. C-H Bond Activation and Catalytic Functionalization I. Springer London, Limited, 2015.
Знайти повний текст джерелаЧастини книг з теми "Catalytic C-H"
Tomin, Anna, Seema Bag, and Béla Török. "Catalytic CH Bond Activation Reactions." In Green Techniques for Organic Synthesis and Medicinal Chemistry, 67–97. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9780470711828.ch4.
Повний текст джерелаGhosh, Pradip, Marc-Etienne Moret, and Robertus J. M. Klein Gebbink. "Catalytic Oxygenation of CC and CH Bonds." In Non-Noble Metal Catalysis, 355–89. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527699087.ch14.
Повний текст джерелаLi, Jie, Suman De Sarkar, and Lutz Ackermann. "meta- and para-Selective C–H Functionalization by C–H Activation." In C-H Bond Activation and Catalytic Functionalization I, 217–57. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_130.
Повний текст джерелаKakiuchi, Fumitoshi, and Shinji Murai. "Activation of C-H Bonds: Catalytic Reactions." In Activation of Unreactive Bonds and Organic Synthesis, 47–79. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-68525-1_3.
Повний текст джерелаKakiuchi, Fumitoshi. "Catalytic Addition of C – H Bonds to C – C Multiple Bonds." In Topics in Organometallic Chemistry, 1–33. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/3418_2007_064.
Повний текст джерелаLiu, Zhanxiang, and Yuhong Zhang. "Catalytic C-H Bond Cleavage for Heterocyclic Compounds." In Green Techniques for Organic Synthesis and Medicinal Chemistry, 131–59. Chichester, UK: John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119288152.ch7.
Повний текст джерелаSustac Roman, Daniela, and André B. Charette. "Catalytic C–H Bond Functionalization of Cyclopropane Derivatives." In Topics in Organometallic Chemistry, 91–113. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_118.
Повний текст джерелаDana, Suman, M. Ramu Yadav, and Akhila K. Sahoo. "Ruthenium-Catalyzed C−N and C−O Bond-Forming Processes from C−H Bond Functionalization." In C-H Bond Activation and Catalytic Functionalization I, 189–215. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_126.
Повний текст джерелаWencel-Delord, Joanna, Frederic W. Patureau, and Frank Glorius. "Rh(III)- and Ir(III)-Catalyzed C–C Bond Cross Couplings from C–H Bonds." In C-H Bond Activation and Catalytic Functionalization I, 1–27. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_140.
Повний текст джерелаDailler, David, Grégory Danoun, and Olivier Baudoin. "Applications of Catalytic Organometallic C(sp3)–H Bond Functionalization." In Topics in Organometallic Chemistry, 133–53. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_122.
Повний текст джерелаТези доповідей конференцій з теми "Catalytic C-H"
SANFORD, MELANIE. "CONTROLLING SELECTIVITY AND REACTIVITY IN CATALYTIC C–H FUNCTIONALIZATION REACTIONS." In 24th International Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2018. http://dx.doi.org/10.1142/9789813237179_0003.
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 джерелаLe, Anh Ngoc Tram, Hung Hoa Lam, Tuyet Mai Tran Thuy, Long Quang Nguyen, Ngo Tran Hoang Duong, Thuan Minh Nguyen, and Dung Van Nguyen. "Facile Preparation of Multifunctional Ag-Fe<sub>x</sub>O<sub>y</sub>/C Composite from Coffee Husk for Antibacterial and Catalytic Applications." In 5th International Conference on Advanced Materials Science. Switzerland: Trans Tech Publications Ltd, 2023. http://dx.doi.org/10.4028/p-58b9m3.
Повний текст джерелаHui, K. S., and Christopher Y. H. Chao. "Conversion of Coal Fly Ash Into Zeolite 4A and Its Applications in Waste Water Treatment and Greenhouse Gas Reduction." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-41361.
Повний текст джерелаCirujano, Francisco. "Ionic liquids vs. microporous solids as reusable reaction media for the catalytic C–H functionalization of indoles with alcohols." In The 22nd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2018. http://dx.doi.org/10.3390/ecsoc-22-05655.
Повний текст джерелаYin, Sudong, Yanglin Pan, and Zhongchao Tan. "Catalytic Hydrothermal Conversion of Glucose to Light Petroleum Alkanes." In ASME 2010 4th International Conference on Energy Sustainability. ASMEDC, 2010. http://dx.doi.org/10.1115/es2010-90433.
Повний текст джерелаDumeignil, Franck, Benjamin Katryniok, and Negissa Ebadi Pour. "Glycerol polymerization over stable and selective calcium hydroxyapatite." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/dpka8345.
Повний текст джерелаChen, Guanyi, Qiang Li, Xiaoyang Lv, Na Deng, and Lifei Jiao. "Production of Hydrogen-Rich Gas Through Pyrolysis of Biomass in a Two-Stage Reactor." In ASME Turbo Expo 2004: Power for Land, Sea, and Air. ASMEDC, 2004. http://dx.doi.org/10.1115/gt2004-53582.
Повний текст джерелаDavison, Evan, Jessica Otto, Sandeep Kumar, and Randy Maglinao. "Production of Branched Esters via Continuous Alkylation of Fatty Acid Methyl Esters over Montmorillonite and h-zsm5 Catalysts." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/ezak5028.
Повний текст джерелаAmama, Placidus B., Jonathan E. Spowart, Andrey A. Voevodin, and Timothy S. Fisher. "Modified Magnesium Hydride and Calcium Borohydride for High-Capacity Thermal Energy Storage." In ASME/JSME 2011 8th Thermal Engineering Joint Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/ajtec2011-44133.
Повний текст джерелаЗвіти організацій з теми "Catalytic C-H"
Crabtree, Robert. Moving to Sustainable Metals: Multifunctional Ligands in Catalytic, Outer Sphere C-H, N-H and O-H Activation. Office of Scientific and Technical Information (OSTI), March 2015. http://dx.doi.org/10.2172/1171638.
Повний текст джерела