Добірка наукової літератури з теми "Alkoxylation"
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Статті в журналах з теми "Alkoxylation"
Liu, Zhuqing, Fei Huang, Jiang Lou, Quannan Wang, and Zhengkun Yu. "Copper-promoted direct C–H alkoxylation of S,S-functionalized internal olefins with alcohols." Organic & Biomolecular Chemistry 15, no. 26 (2017): 5535–40. http://dx.doi.org/10.1039/c7ob01234a.
Повний текст джерелаShen, Jiabin, Jun Xu, Heng Cai, Chao Shen, and Pengfei Zhang. "Platinum(ii)-catalyzed selective para C–H alkoxylation of arylamines through a coordinating activation strategy." Organic & Biomolecular Chemistry 17, no. 3 (2019): 490–97. http://dx.doi.org/10.1039/c8ob02942c.
Повний текст джерелаLin, John, Upali Weerasooriya, E. Leach Bruce, Steve V. Orsak, and Park T. X. Cedar. "5627121 Process for preparing alkoxylation catalysts and alkoxylation process." Journal of Molecular Catalysis A: Chemical 125, no. 2-3 (November 1997): 182. http://dx.doi.org/10.1016/s1381-1169(98)80116-7.
Повний текст джерелаLiu, Lunzu, Guowei Li, and Mingzhi Huang. "ALKOXYLATION OF HYDRIDOPHOSPHORANES." Phosphorus, Sulfur, and Silicon and the Related Elements 69, no. 1-2 (June 1992): 1–6. http://dx.doi.org/10.1080/10426509208036849.
Повний текст джерелаWeerasooriya, Upali. "Ester alkoxylation technology." Journal of Surfactants and Detergents 2, no. 3 (July 1999): 373–81. http://dx.doi.org/10.1007/s11743-999-0092-5.
Повний текст джерелаLakhtin, V. G., V. L. Ryabkov, M. V. Polyakova, V. M. Nosova, A. F. Kisin, and E. A. Chernyshev. "Alkoxylation ofC-chlorovinylsilanes." Russian Chemical Bulletin 44, no. 4 (April 1995): 718–23. http://dx.doi.org/10.1007/bf00698510.
Повний текст джерелаRogers, R. L., and K. Hermann. "Upgrading an Alkoxylation Facility." Process Safety and Environmental Protection 82, no. 1 (January 2004): 12–17. http://dx.doi.org/10.1205/095758204322777624.
Повний текст джерелаRomanova, S. M., A. M. Madyakina, L. A. Fatykhova, and S. V. Fridland. "Alkoxylation of cellulose nitrates." Russian Journal of General Chemistry 83, no. 1 (January 2013): 58–62. http://dx.doi.org/10.1134/s1070363213010106.
Повний текст джерелаZhang, Yu-Feng, and Mohamed Mellah. "Samarium(ii)-electrocatalyzed chemoselective reductive alkoxylation of phthalimides." Organic Chemistry Frontiers 9, no. 5 (2022): 1308–14. http://dx.doi.org/10.1039/d1qo01760h.
Повний текст джерелаTakemura, Noriaki, Yoichiro Kuninobu, and Motomu Kanai. "Copper-catalyzed benzylic C(sp3)–H alkoxylation of heterocyclic compounds." Org. Biomol. Chem. 12, no. 16 (2014): 2528–32. http://dx.doi.org/10.1039/c4ob00215f.
Повний текст джерелаДисертації з теми "Alkoxylation"
Arbour, Jannine Louise. "Metal-mediated intramolecular hydroamination and hydro(acy)alkoxylation reactions." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/9203.
Повний текст джерелаDiamante, Daria. "Transition metal-catalyzed alkoxylation and amination reactions involving propargyl or allyl derivatives." Thesis, Paris 6, 2017. http://www.theses.fr/2017PA066119/document.
Повний текст джерелаDuring the whole period of my PhD, spent in co-tutorship between Università degli Studi dell’Insubria and UPMC in Paris, I have directed my efforts towards the study of C-O and C-N bonds formation by new transition metal-catalyzed reactions.Pursuing our ongoing project on intra- and intermolecular transition metal-catalyzed amination and alkoxylation reactions involving C-H functionalization, we tried to perform two intramolecular alkoxylation procedures of carbon-carbon multiple bonds to obtain oxygenated heterocycles and one intermolecular oxidative allylic amination to accomplish nitrogen-based scaffolds.Performed at intramolecular level, transition metal-catalyzed reactions offer a versatile strategy to obtain cyclic molecules, not easily obtainable by conventional synthetic methods and starting from readily available starting materials, and represent one of the key methodologies for the progress of green and sustainable chemistry. Dealing with alkoxylation protocols, two different research lines based on transition metal catalysis applied to domino reactions were investigated. Domino processes are efficient tools to rapidly increase the molecular complexity through the formation of more than one bond in a single step, respecting the rule of step economy. While the domino approach involving alkenes and allenes is well investigated, examples involving alkynes are somewhat limited in the literature
Moradi, Alfred. "Organic synthesis via anodically generated iminium cations." Thesis, Queen Mary, University of London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297194.
Повний текст джерелаGIOFRE', SABRINA. "SYNTHESIS OF NITROGEN-CONTAINING HETEROCYCLIC SYSTEMS OF BIOLOGICAL INTEREST THROUGH DOMINO STRATEGIES." Doctoral thesis, Università degli Studi di Milano, 2020. http://hdl.handle.net/2434/701960.
Повний текст джерелаHall, Charles A. "Kinetics and mass-transfer effects in batch alkoxylations." Thesis, Georgia Institute of Technology, 1987. http://hdl.handle.net/1853/11213.
Повний текст джерелаZhang, Shoukun. "Selective C–H Activation by Ruthenium(II) Carboxylate and Nickelaelectro-Catalysis." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2021. http://hdl.handle.net/21.11130/00-1735-0000-0005-155B-E.
Повний текст джерелаSmith, Paul Craig. "The alkoxylation of biodiesel and its impact on fuel properties." Thesis, 2010. http://hdl.handle.net/2440/61635.
Повний текст джерелаThesis (Ph.D.) -- University of Adelaide, School of Chemical Engineering, 2010
Yen-Yi, Hu, та 胡衍毅. "Asymmetric electro-oxidative intramolecular α-alkoxylation of Pyrrolidine : The Synthesis of (-)-Pyrrolidine 197 B And The Synthesis of Trachelanthamidine". Thesis, 2000. http://ndltd.ncl.edu.tw/handle/20378772889149665288.
Повний текст джерелаLanier, Megan. "Method Development for the Stereoselective Synthesis of Medium-Sized Cyclic Ethers and Application to Natural Product Synthesis: Part I. Organocatalytic Oxa-Conjugate Addition for α,α´-trans-Oxepanes Part II. Gold(I)-Catalyzed Alkoxylation for α,α´-cis-Oxocenes Part III. Studies toward the Synthesis." Diss., 2015. http://hdl.handle.net/10161/9941.
Повний текст джерелаMedium-sized cyclic ethers are challenging synthetic targets due to enthalpic and entropic barriers. Methods for the stereoselective synthesis of α,α΄-disubstituted medium-sized cyclic ethers began to appear with the discovery of naturally-occurring, ladder-shaped polycyclic ethers, such as brevetoxin B, and monocyclic ethers, such as (+)-laurencin. Despite the progress made in this field, limitations remain including competing formation of smaller ring sizes and scarcity of catalytic methods. Our aim has been to develop stereoselective syntheses for 7- and 8-membered cyclic ethers which have potential for application in natural product synthesis. The C-O bond disconnection was selected for the methods described within because cyclization and stereoinduction could be achieved simultaneously. In the case of 7-membered cyclic ethers, an organocatalytic oxa-conjugate addition reaction promoted by the gem-disubstituent (Thorpe−Ingold) effect has been developed to stereoselectively provide α,α′-trans-oxepanes. A gold(I)-catalyzed alkoxylation reaction has also allowed access to α,α′-cis-oxocenes. This method has been probed for feasibility in the stereoselective synthesis of (+)-intricenyne, an 8-membered cyclic ether belonging to the C15 nonterpenoid acetogenin natural product class. These methods have the potential to become general and efficient routes to highly functionalized oxepanes and oxocenes.
Dissertation
Частини книг з теми "Alkoxylation"
Caiado, M., D. S. Pito, and J. E. Castanheiro. "Alkoxylation of Terpenes over Tungstophosphoric Acid Immobilised on Silica Support." In Environmentally Benign Catalysts, 153–64. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6710-2_7.
Повний текст джерелаStadlbauer, W. "Alkoxylation." In Five-Membered Hetarenes with Two Nitrogen or Phosphorus Atoms, 1. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-012-00362.
Повний текст джерелаSapeta, K., and M. A. Kerr. "Alkoxylation." In Science of Synthesis Knowledge Updates KU 2011/1, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-112-00091.
Повний текст джерелаCamp, J. E. "C-Alkoxylation." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles, 1. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00064.
Повний текст джерелаSoenen, D. R., and C. D. Vanderwal. "Photochemical Alkoxylation." In Ethers, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-037-00108.
Повний текст джерелаSato, N. "Hydroxylation and Alkoxylation." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00974.
Повний текст джерелаSato, N. "Hydroxylation, Alkoxylation, and Sulfanylation." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-116-00487.
Повний текст джерелаSoenen, D. R., and C. D. Vanderwal. "Radical Alkoxylation of Alkenes." In Ethers, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-037-00113.
Повний текст джерелаSoenen, D. R., and C. D. Vanderwal. "Electrochemical Alkoxylation of Alkenes." In Ethers, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-037-00114.
Повний текст джерелаSato, N. "Hydroxylation, Alkoxylation, and Sulfanylation." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00986.
Повний текст джерелаТези доповідей конференцій з теми "Alkoxylation"
Carreira de Rezende, Fabiola, Rodrigo Balloni Rabelo, Lilian Kinouti, Conrado Gerard Ewbank, and Olivia Cueva Candido Poltronieri. "Tailoring Alkoxylation of Flowback Aid Surfactants for Maximum Efficiency." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2019. http://dx.doi.org/10.2118/193623-ms.
Повний текст джерелаNohr, Marcus, Tilman Utz, and Knut Graichen. "Kinetic modelling of an industrial semi-batch alkoxylation reactor for control studies." In 2014 UKACC International Conference on Control (CONTROL). IEEE, 2014. http://dx.doi.org/10.1109/control.2014.6915210.
Повний текст джерелаXu, Zhen, Jinsheng Zhao, and Weiyu Fan. "Chemosynthesis and photoelectric characterization of a novel solution-processable electrochromic copolymer based on alternating alkoxylating benzene and benzo[1,2-b:4,5-b']dithiophene derivatives." In 2015 2nd International Workshop on Materials Engineering and Computer Sciences. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/iwmecs-15.2015.120.
Повний текст джерела