Диссертация (1150063), страница 25

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I., Kukushkin, V. Y., Haukka, M. Hydrogen bondingpatterns in pyrazole Pt(II- and IV) chloride complexes. // Inorganica Chimica Acta– 2006 – 359 – p. 320−326.66.Vignolle, J., Catton, X., Bourissou, D. Stable noncyclic singlet carbenes. // Chem.Rev. – 2009 – 109 – p. 3333–3384.67.Bondi, A. Van der Waals Volumes and Radii. // J. Phys. Chem.

– 1964 – 68 –p. 441–451.68.Zhong, Y.-R., Cao, M.-L., Mo, H.-J., Ye, B.-H. Syntheses and Crystal Structures ofMetal Complexes with 2,2′-Biimidazole-like Ligand and Chloride: Investigation ofX−H···Cl (X = N, O, and C) Hydrogen Bonding and Cl−π (imidazolyl)Interactions. // Crystal Growth & Design – 2008 – 8 – p. 2282−2290.69.Dinda, J., Das, D., Santra, P. K., Sinha, C., Falvello, L. R.

Cyclopalladation versushydroxylation. A case of pH dependence. // J. Organomet. Chem. – 2001 – 629 –p. 28–38.70.IUPAC. A Guide to IUPAC Nomenclature of Organic Compounds(Recommendations 1993): Blackwell Scientific publications, 1993. p.71.Michelin, R. A., Sgarbossa, P., Sbovata, S. M., Gandin, V., Marzano, C., Bertani,R. Chemistry and Biological Activity of Platinum Amidine Complexes. //ChemMedChem – 2011 – 6 – p. 1172–1183.72.Osakada, K., Yamamoto, T. Transmetallation of Alkynyl and Aryl Complexes ofGroup 10 Transition Metals. // Coord.

Chem. Rev. – 2000 – 198 – p. 379–399.73.Hartley, F. R. The Chemistry of Platinum and Palladium – London: AppliedScience Publishers, Ltd, 1973. p.74.Harding, D. J., Saithong, S., Pakawatchai, C., Youngme, S. transDichloro(triethylamine-[kappa]N)(triphenylphosphine-[kappa]P)palladium(II). //142Acta Crystallogr.

E – 2006 – 62 – p. m1616–m1617.75.Slaughter, L. M. Acyclic Aminocarbenes in Catalysis. // ACS Catal. – 2012 – 2 –p. 1802–1816.76.Chanda, A., Fokin, V. A. Organic synthesis “on water”. // Chem. Rev. – 2009 –109 – p. 725–748.77.Chalker, J. M., Wood, C. S. C., Davis, B. G. A convenient catalyst for aqueous andprotein Suzuki–Miyaura cross-coupling.

// J. Am. Chem. Soc. – 2009 – 131 –p. 16346–16347.78.Spicer, C. D., Davis, B. G. Palladium-mediated site-selective Suzuki–Miyauraprotein modification at genetically encoded aryl halides. // Chem. Commun. – 2011– p. 1698–1700.79.Casalnuovo, A. L., Calabrese, J. C. Palladium-Catalyzed Alkylations in AqueousMedia. // J. Am. Chem. Soc. – 1990 – 112 – p. 4324–4330.80.Cornils, B., Herrmann, W. A.

Aqueous-phase organometallic catalysis: conceptsand applications. 2nd ed – Weinheim, Germany: Wiley-VCH, 2004. p.81.Joo, F. Aqueous organometallic catalysis – Dordrecht, The Netherlands: Kluwer, 2001.82.Godoy, F., Segarra, C., Poyatos, M., Peris, E. Palladium Catalysts with SulfonateFunctionalized-NHC Ligands for Suzuki−Miyaura Cross-Coupling Reactions inWater. // Organometallics – 2011 – 30 – p. 684–688.83.Moseley, J. D., Murray, P. M., Turp, E. R., Tyler, S.

N. G., Burn, R. T. A mildrobust generic protocol for the Suzuki reaction using an air stable catalyst. //Tetrahedron – 2012 – 68 – p. 6010–6017.84.Wei, J.-F., Jiao, J., Feng, J.-J., Lv, J., Zhang, X.-R., Shi, X.-Y., Chen, Z.-G. PdEDTAHeld in an Ionic Liquid Brush as a Highly Efficient and Reusable Catalyst for SuzukiReactions in Water.

// J. Org. Chem. – 2009 – 74 – p. 6283–6286.85.Костиков, Р. Р., Кузнецов, М. А., Новиков, М. С., Соколов, В. В., Хлебников,А. Ф. Практикум по органическому синтезу – СПб: ВВМ, 2009. p.86.Chattopadhyay, P., Nagpal, R., Pandey, P. S. Recognition Properties of FlavinAnalogues with Bile Acid-Based Receptors: Role of Steric Effects in HydrogenBond Based Molecular Recognition.

// Australian Journal of Chemistry – 2008 – 61– p. 216–222.87.Gabe, Y., Urano, Y., Kikuchi, K., Kojima, H., Nagano, T. Highly SensitiveFluorescence Probes for Nitric Oxide Based on Boron DipyrrometheneChromophoreRational Design of Potentially Useful Bioimaging FluorescenceProbe. // Journal of the American Chemical Society – 2004 – 126 – p. 3357–3367.88.Rüchardt, C., Hassmann, V.

Aromatische Diazoniumsalze, X. Durchführung derJacobsonschen Indazolsynthese im Eintopfverfahren. // Liebigs Annalen derChemie – 1980 – 1980 – p. 908–927.143.

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