Εμφανίζονται 1 - 20 Αποτελέσματα από 34 για την αναζήτηση '"Кросс-сочетание"', χρόνος αναζήτησης: 0,61δλ Περιορισμός αποτελεσμάτων
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    Academic Journal

    Πηγή: Proceedings of the National Academy of Sciences of Belarus, Chemical Series; Том 57, № 1 (2021); 7-14 ; Известия Национальной академии наук Беларуси. Серия химических наук; Том 57, № 1 (2021); 7-14 ; 2524-2342 ; 1561-8331 ; 10.29235/1561-8331-2021-57-1

    Περιγραφή αρχείου: application/pdf

    Relation: https://vestichem.belnauka.by/jour/article/view/625/595; Vul', A. Detonation Nanodiamonds: Science and Applications / A. Vul', O. Shenderova. - Boca Raton: Pan Stanford Publishing, 2013. - 346p. https://doi.org/10.1201/b15541; Williams, O. A. Nanodiamond / O. A. Williams. - London: The Royal Society of Chemistry, 2014. - 530 p. https://doi.org/10.1039/9781849737616; Ho, D. Nanodiamonds: Applications in Biology and Nanoscale Medicine / D. Ho. - N. Y.: Springer Science + Business Media, 2010. - 286 p. https://doi.org/10.1007/978-1-4419-0531-4; The properties and applications of nanodiamonds / V. N. Mochalin [et al.] // Nature Nanotech. - 2012. - Vol 7, N 1. -P. 11-23. https://doi.org/10.1038/nnano.2011.209; Arnault, J.-C. Nanodiamonds / J.-C. Arnault. - London: Elsevier, 2017. - 514.; Turcheniuk, K. Biomedical applications of nanodiamond / K. Turcheniuk, V. Mochalin // Nanotechnology. - 2017. -Vol. 28, N 25. - P. 252001. https://doi.org/10.1088/1361-6528/aa6ae4; Mochalin, V. N. Covalent Incorporation of Aminated Nanodiamond into an Epoxy Polymer Network / V. N. Mochalin // ACS Nano. - 2011. - Vol. 5, N 9. - P. 7494-7502. https://doi.org/10.1021/nn2024539; Dolmatov, V. Y. Detonation nanodiamonds in oils and lubricants / V. Y. Dolmatov // J. Superhard Mater. - 2010. -Vol. 32, N 1. - P. 14-20. https://doi.org/10.3103/s1063457610010028; Chauhan, S. Nanodiamonds with powerful ability for drug delivery and biomedical applications: Recent updates on in vivo study and patents / S. Chauhan, N. G. Jain, U. Nagaich // J. Pharm. Anal. - 2020. - Vol. 10, N 1. - P. 1-12. https://doi.org/10.1016/j.jpha.2019.09.003; Moghimi, S. M. Nanoparticle transport pathways into tumors / S. M. Moghimi, D. Simberg // J. Nanopart. Res. -2018. - Vol. 20, N 169. - P. 168-172. https://doi.org/10.1007/s11051-018-4273-8; Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors / S. Haziza [et al.] // Nat. Nanotechnol. - 2017. - Vol. 12, N 4. - P. 322-328. https://doi.org/10.1038/nnano.2016.260; Whitlow, J. Multifunctional nanodiamonds in regenerative medicine: Recent advances and future directions / J. Whitlow, S. Pacelli, A. Paul // J. Control. Release. - 2017. - N 261. - P. 62-86. https://doi.org/10.1016/j.jconrel.2017.05.033; Serp, P. Carbon Materials for Catalysis / P. Serp, J. L. Figueiredo. - Oxford: John Wiley & Sons, 2009. - 589 p. https://doi.org/10.1002/9780470403709; Reduction of nitrobenzene catalyzed by carbon materials / S. Wu [et al.] // Chin. J. Catal. -2014. - Vol. 35, N 6. -P. 914-921. https://doi.org/10.1016/S1872-2067(14)60102-9; Palladium on ultradisperse diamond and activated carbon: the relation between structure and activity in hydrodechlorination / S. A. Kachevskii, [et al.] // Russ. J. Phys. Chem. - 2007. - Vol. 81, N 6. - P. 866-873. https://doi.org/10.1134/S0036024407060064; Synthesis and application of gold-carbon hybrids as catalysts for the hydroamination of alkynes / Seral-Ascaso [et al.] // Appl. Catal. A: Gen. - 2013. - Vol. 456. - P. 88-95. https://doi.org/10.1016/j.apcata.2013.02.008; Arsenazo III and its analogues-VI* Some new photometric reagents for palladium / S. B. Savvin [et al.] // Talanta. -1969. - Vol. 16. - P. 423-429. https://doi.org/10.1016/0039-9140(69)80036-6; https://vestichem.belnauka.by/jour/article/view/625

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    Academic Journal

    Πηγή: Proceedings of the National Academy of Sciences of Belarus, Chemical Series; Том 55, № 2 (2019); 196-204 ; Известия Национальной академии наук Беларуси. Серия химических наук; Том 55, № 2 (2019); 196-204 ; 2524-2342 ; 1561-8331 ; 10.29235/1561-8331-2019-55-2

    Time: 1

    Περιγραφή αρχείου: application/pdf

    Relation: https://vestichem.belnauka.by/jour/article/view/391/369; Choi S. K. Mechanistic basis of light induced cytotoxicity of photoactive nanomaterials. NanoImpact, 2016, vol. 3–4, pp. 81–89. https://doi.org/10.1016/j.impact.2016.09.001; Yola M. L., Eren T., Atar N. A novel effcient photocatalyst based on TiO2 nanoparticles involved boron enrichment waste for photocatalytic degradation of atrazine. Chem. Eng. J., 2014, vol. 250, pp. 288–294. https://doi.org/10.1016/j.cej.2014.03.116; Yola M. L., Eren T., Atar N. A sensitive molecular imprinted electrochemical sensor based on gold nanoparticles decorated graphene oxide: Application to selective determination of tyrosine in milk. Sens. Actuators B Chem., 2015, vol. 210, pp. 149–157. https://doi.org/10.1016/j.snb.2014.12.098; Beytur M., Kardas F., Akyildirim O., Ozkan A., Bankoglu B., Yuksek H., Yola M. L., Atar N. A highly selective and sensitive voltammetric sensor with molecularly imprinted polymer based silver@gold nanoparticles/ionic liquid modifed glassy carbon electrode for determination of ceftizoxime. J. Mol. Liq., 2018, vol. 251, pp. 212–217. https://doi.org/10.1016/j.molliq.2017.12.060; Barbaro P., Liguori F. Ion Exchange Resins: Catalyst Recovery and Recycle. Chem. Rev., 2009, vol. 109, no. 2, pp. 515–529. https://doi.org/10.1021/cr800404j; Kazmaier U., Pohlman M. Cross-Coupling Reactions via π-Allyl Metal Intermediates / U. Kazmaier, M. Pohlman // MetalCatalyzed Cross-Coupling Reactions / Wiley-VCH; A. de Meijere, F. Diederich (Eds.). – Weinheim, 2004. – P. 531–583.; Chartoire A., Nolan S.P. Advances in C–C and C–X Coupling Using Palladium-N-Heterocyclic Carbene (Pd-NHC) Complexes / A. Chartoire, S.P. Nolan // New Trends in Cross-Coupling: Theory and Applications / Royal Society of Chemistry; J. Spivey [et al.] (Eds.). – Cambridge, 2014. – P. 139–219.; Jekab A., Dalicsek Z., Holczbauer T., Hamza A., Papai I., Finta Z., Timari G., Soos T. Superstable Palladium(0) Complex as an Air- and Thermostable Catalyst for Suzuki Coupling Reactions. Eur. J. Org. Chem., 2015. vol. 2015, no. 1, pp. 60–66. https://doi.org/10.1002/ejoc.201403214; Cantillo D., Kappe C. O. Immobilized Transition Metals as Catalysts for Cross-Couplings in Continuous Flow-A Critical Assessment of the Reaction Mechanism and Metal Leaching. ChemCatChem., 2014, vol. 6, no. 12, pp. 3286–3305. https://doi.org/10.1002/cctc.201402483; Becht J. M., le Drian C. Biaryl Synthesis via Decarboxylative Pd-Catalyzed Reactions of Arenecarboxylic Acids and Diaryliodonium Triflates. Org. Lett., 2008, vol. 10, no. 14, pp. 3161–3164. https://doi.org/10.1021/ol8011293; Farrusseng D., Tuel A. Perspectives on zeolite-encapsulated metal nanoparticles and their applications in catalysis. New J. Chem., 2016, vol. 40, no. 5, pp. 3933–3949. https://doi.org/10.1039/C5NJ02608C; Kalidindi S. B., Nayak S., Briggs M. E., Jansat S., Katsoulidis A. P., Miller G. J., Warren J. E., Antypov D., Cora F., Slater B., Prestly M. R., Marti-Gastaldo C., Rosseinsky M. J. Chemical and Structural Stability of Zirconium-based Metal–Organic Frameworks with Large Three-Dimensional Pores by Linker Engineering. Angew. Chem. Int. Ed. Engl., 2015, vol. 54, no. 1, pp. 221–226. https://doi.org/10.1002/anie.201406501; Gaponik P. N., Ivashkevich O. A., Karavai V. P., Lesnikovich A. I., Chernavina N. I., Sukhanov G. T., Gareev G. A. Polymers and copolymers based on vinyl tetrazoles, 1*. Synthesis of poly(5-vinyl tetrazole) by polymer-analogous conversion of polyacrylonitrile. Angew. Makromol. Chem., 1994, vol. 219, no. 1, pp. 77–88. https://doi.org/10.1002/apmc.1994.052190107; Zuraev A. V., Grigoriev Y. V., Ivashkevich L. S., Lyakhov A. S., Ivashkevich O. A. Copper-Polymer Nanocomposite Catalyst for Synthesis of 1,4-Diphenylbutadiyne-1,3. Z. Anorg. Allg. Chem., 2017, vol. 643, no. 19, pp. 1215–1219. https://doi.org/10.1002/zaac.201700213; Zuraev A. V., Grigoriev Y. V., Budevich V. A., Ivashkevich O. A. Copper-polymer nanocomposite: An effcient catalyst for green Huisgen click synthesis. Tetrahedron Lett., 2018, vol. 59, no. 16, pp. 1583–1586. https://doi.org/10.1016/j.tetlet.2018.03.028; Levchik S. V., Bolvanovich E. E., Lesnikovich A. I., Ivashkevich O. A., Gaponik P. N., Vyazovakin S. V. Thermal decomposition of tetrazole-containing polymers. I. Poly-5-vinyltetrazole thermolysis. Thermochim. Acta., 1990, vol. 168, pp. 211–221. https://doi.org/10.1016/0040-6031(90)80640-K; https://vestichem.belnauka.by/jour/article/view/391

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    Academic Journal

    Συνεισφορές: Казанский (Приволжский) федеральный университет

    Relation: ИТОГОВАЯ НАУЧНО-ПРАКТИЧЕСКАЯ КОНФЕРЕНЦИЯ ПРОФЕССОРСКО-ПРЕПОДАВАТЕЛЬСКОГО СОСТАВА ИНСТИТУТА ФИЗИКИ И ХИМИЧЕСКОГО ИНСТИТУТА ИМЕНИ А.М. БУТЛЕРОВА КАЗАНСКОГО ФЕДЕРАЛЬНОГО УНИВЕРСИТЕТА; http://dspace.kpfu.ru/xmlui/bitstream/net/175779/-1/F_ktk2022_129.pdf; https://dspace.kpfu.ru/xmlui/handle/net/175779; 547.6

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    Conference

    Περιγραφή αρχείου: application/pdf

    Relation: Актуальные вопросы органической химии и биотехнологии. — Екатеринбург, 2020; http://elar.urfu.ru/handle/10995/135130

    Διαθεσιμότητα: http://elar.urfu.ru/handle/10995/135130

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    Conference

    Περιγραφή αρχείου: application/pdf

    Relation: Актуальные вопросы органической химии и биотехнологии. — Екатеринбург, 2020; http://elar.urfu.ru/handle/10995/96900

    Διαθεσιμότητα: http://elar.urfu.ru/handle/10995/96900

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    Conference

    Περιγραφή αρχείου: application/pdf

    Relation: info:eu-repo/grantAgreement/RSF//16-13-10331; Актуальные вопросы органической химии и биотехнологии. — Екатеринбург, 2020; http://elar.urfu.ru/handle/10995/96862

    Διαθεσιμότητα: http://elar.urfu.ru/handle/10995/96862

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