Фосфонаты фенантролинового ряда в создании регенерируемых катализаторов для процессов зеленой химии, страница 26
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2011, 47,5611-5613.61.Do, H.-Q. and Daugulis, O. A General Method for Copper-Catalyzed Arene CrossDimerization. // J. Am. Chem. Soc. 2011, 133, 13577-13586.62.Oishi, M.; Kondo, H. and Amii, H. Aromatic trifluoromethylation catalytic in copper. // Chem.Comm. 2009, 1909-1911.63.Knauber, T.; Arikan, F.; Röschenthaler, G.-V. and Gooßen, L.J. Copper-CatalyzedTrifluoromethylation of Aryl Iodides with Potassium (Trifluoromethyl)trimethoxyborate. //Chem. – Eur. J. 2011, 17, 2689-2697.64.Kondo, H.; Oishi, M.; Fujikawa, K.
and Amii, H. Copper-Catalyzed AromaticTrifluoromethylation via Group Transfer from Fluoral Derivatives. // Adv. Synth. Catal. 2011,353, 1247-1252.14165.Liu, T. and Shen, Q. Copper-Catalyzed Trifluoromethylation of Aryl and Vinyl Boronic Acidswith An Electrophilic Trifluoromethylating Reagent. // Org. Lett.
2011, 13, 2342-2345.66.Chu, L. and Qing, F.-L. Copper-Mediated Oxidative Trifluoromethylation of Boronic Acids. //Org. Lett. 2010, 12, 5060-5063.67.Senecal, T.D.; Parsons, A.T. and Buchwald, S.L. Room Temperature Aryl Trifluoromethylationvia Copper-Mediated Oxidative Cross-Coupling. // J. Org. Chem. 2011, 76, 1174-1176.68.Chu, L. and Qing, F.-L.
Copper-Catalyzed Direct C–H Oxidative Trifluoromethylation ofHeteroarenes. // J. Am. Chem. Soc. 2011, 134, 1298-1304.69.Chu, L. and Qing, F.-L. Copper-Mediated Aerobic Oxidative Trifluoromethylation of TerminalAlkynes with Me3SiCF3. // J. Am. Chem. Soc. 2010, 132, 7262-7263.70.Mao, Z.; Huang, F.; Yu, H.; Chen, J.; Yu, Z. and Xu, Z. Copper-CatalyzedTrifluoromethylation of Internal Olefinic C H Bonds: Efficient Routes to TrifluoromethylatedTetrasubstituted Olefins and N-Heterocycles.
// Chem. – Eur. J. 2014, 20, 3439-3445.71.Popov, I.; Lindeman, S. and Daugulis, O. Copper-Catalyzed Arylation of 1H-Perfluoroalkanes.// J. Am. Chem. Soc. 2011, 133, 9286-9289.72.Kern, J.-M. and Sauvage, J.-P. Photoassisted C-C coupling via electron transfer to benzylichalides by a bis(di-imine) copper(I) complex.
// J. Chem. Soc., Chem. Comm. 1987, 546-548.73.Pirtsch, M.; Paria, S.; Matsuno, T.; Isobe, H. and Reiser, O. [Cu(dap)2Cl] As an EfficientVisible-Light-Driven Photoredox Catalyst in Carbon–Carbon Bond-Forming Reactions. //Chem. – Eur. J. 2012, 18, 7336-7340.74.Gooßen, L.J.; Rodríguez, N.; Manjolinho, F. and Lange, P.P. Synthesis of Propiolic Acids viaCopper-Catalyzed Insertion of Carbon Dioxide into the C H Bond of Terminal Alkynes. //Adv. Synth.
Catal. 2010, 352, 2913-2917.75.Karlstedt, N.B. and Beletskaya, I.P. Copper-catalyzed cross-coupling of diethyl phosphonatewith aryl iodides. // Russ. J. Org. Chem. 2011, 47, 1011-1014.76.Zhuang, R.; Xu, J.; Cai, Z.; Tang, G.; Fang, M. and Zhao, Y. Copper-Catalyzed C−P BondConstruction via Direct Coupling of Phenylboronic Acids with H-Phosphonate Diesters. // Org.Lett. 2011, 13, 2110-2113.77.Hu, J.; Zhao, N.; Yang, B.; Wang, G.; Guo, L.-N.; Liang, Y.-M. and Yang, S.-D. CopperCatalyzed C–P Coupling through Decarboxylation.
// Chem. – Eur. J. 2011, 17, 5516-5521.78.Bernoud, E.; Alayrac, C.; Delacroix, O. and Gaumont, A.-C. Copper-catalyzed synthesis ofalkynylphosphine derivatives: unprecedented use of nucleophilic phosphorus compounds. //Chem. Comm. 2011, 47, 3239-3241.14279.Zhao, D.; Wu, N.; Zhang, S.; Xi, P.; Su, X.; Lan, J. and You, J. Synthesis of Phenol, AromaticEther, and Benzofuran Derivatives by Copper-Catalyzed Hydroxylation of Aryl Halides. //Angew. Chem., Int.
Ed. 2009, 48, 8729-8732, S8729/8721-S8729/8730.80.Tao, C.Z.; Liu, W.W. and Sun, J.Y. Copper-catalyzed synthesis of phenols from aryl halidesand 4-methoxybenzyl alcohol. // Chin. Chem. Lett. 2009, 20, 1170-1174.81.Wolter, M.; Nordmann, G.; Job, G.E. and Buchwald, S.L. Copper-Catalyzed Coupling of ArylIodides with Aliphatic Alcohols. // Org. Lett. 2002, 4, 973-976.82.Toumi, M.; Couty, F.
and Evano, G. Total synthesis of paliurine F. // Angew. Chem., Int. Ed.2007, 46, 572-575.83.Altman, R.A.; Shafir, A.; Choi, A.; Lichtor, P.A. and Buchwald, S.L. An Improved Cu-BasedCatalyst System for the Reactions of Alcohols with Aryl Halides. // J. Org.
Chem. 2008, 73,284-286.84.Nordmann, G. and Buchwald, S.L. A Domino Copper-Catalyzed C-O Coupling-ClaisenRearrangement Process. // J. Am. Chem. Soc. 2003, 125, 4978-4979.85.Fang, Y. and Li, C. Preference of 4-exo Ring Closure in Copper-Catalyzed IntramolecularCoupling of Vinyl Bromides with Alcohols. // J. Am. Chem. Soc.
2007, 129, 8092-8093.86.Chen, L.; Fang, Y.; Zhao, Q.; Shi, M. and Li, C. Synthesis of multisubstituted furans viacopper-catalyzed intramolecular O-vinylation of ketones with vinyl bromides. // TetrahedronLett. 2010, 51, 3678-3681.87.Bates, C.G.; Gujadhur, R.K. and Venkataraman, D. A General Method for the Formation ofAryl-Sulfur Bonds Using Copper(I) Catalysts. // Org. Lett.
2002, 4, 2803-2806.88.Feng, Y.; Zhao, X.; Wang, J.; Zheng, F. and Xu, H. Copper(I) oxide-catalyzed formation of CS bond mediated by N,N'-type ligand. // Chin. J. Chem. 2009, 27, 2423-2425.89.Ke, F.; Qu, Y.-Y.; Jiang, Z.-Q.; Li, Z.-K.; Wu, D. and Zhou, X.-G. An Efficient CopperCatalyzed Carbon-Sulfur Bond Formation Protocol in Water. // Org. Lett. 2011, 13, 454-457.90.Bates, C.G.; Saejueng, P.; Doherty, M.Q. and Venkataraman, D.
Copper-Catalyzed Synthesisof Vinyl Sulfides. // Org. Lett. 2004, 6, 5005-5008.91.Jiang, B.; Tian, H.; Huang, Z.-G. and Xu, M. Successive Copper(I)-Catalyzed Cross-Couplingsin One Pot: A Novel and Efficient Starting Point for Synthesis of Carbapenems. // Org. Lett.2008, 10, 2737-2740.92.Huang, F. and Batey, R.A. Cross-coupling of organoboronic acids and sulfinate salts usingcatalytic copper(II) acetate and 1,10-phenanthroline: synthesis of aryl and alkenylsulfones.
//Tetrahedron. 2007, 63, 7667-7672.93.Gujadhur, R.K. and Venkataraman, D. A general method for the formation of diaryl selenidesusing copper(I) catalysts. // Tetrahedron Lett. 2003, 44, 81-84.14394.Beletskaya, I.P.; Sigeev, A.S.; Peregudov, A.S. and Petrovskii, P.V. Copper(I)-catalyzedarylselenylation of aryl bromides and iodides. // Tetrahedron Lett. 2003, 44, 7039-7041.95.Hirao, T.; Masunaga, T.; Ohshiro, Y. and Agawa, T. Stereoselective synthesis ofvinylphosphonate. // Tetrahedron Lett.
1980, 21, 3595-3598.96.Hirao, T.; Masunaga, T.; Ohshiro, Y. and Agawa, T. A Novel Synthesis of DialkylArenephosphonates. // Synthesis. 1981, 1981, 56-57.97.Hirao, T.; Masunaga, T.; Yamada, N.; Ohshiro, Y. and Agawa, T. Palladium-catalyzed newcarbon-phosphorus bond formation. // Bull. Chem. Soc.
Jpn. 1982, 55, 909-913.98.Tappe, F.M.J.; Trepohl, V.T. and Oestreich, M. Transition-Metal-Catalyzed C-P CrossCoupling Reactions. // Synthesis. 2010, 2010, 3037-3062.99.Demmer, C.S.; Krogsgaard-Larsen, N. and Bunch, L. Review on Modern Advances ofChemical Methods for the Introduction of a Phosphonic Acid Group. // Chem.
Rev. 2011, 111,7981-8006.100.Prim, D.; Campagne, J.-M.; Joseph, D. and Andrioletti, B. Palladium-catalyzed reactions ofaryl halides with soft, non-organometallic nucleophiles. // Tetrahedron. 2002, 58, 2041-2075.101.Comby, S.; Imbert, D.; Chauvin, A.-S.; Bünzli, J.-C.G.; Charbonnière, L.J. and Ziessel, R.F.Influence of Anionic Functions on the Coordination and Photophysical Properties ofLanthanide(III) Complexes with Tridentate Bipyridines. // Inorg. Chem. 2004, 43, 7369-7379.102.Hu, A.; Yee, G.T. and Lin, W. Magnetically Recoverable Chiral Catalysts Immobilized onMagnetite Nanoparticles for Asymmetric Hydrogenation of Aromatic Ketones. // J. Am. Chem.Soc.
2005, 127, 12486-12487.103.Evans, O.R.; Ngo, H.L. and Lin, W. Chiral Porous Solids Based on Lamellar LanthanidePhosphonates. // J. Am. Chem. Soc. 2001, 123, 10395-10396.104.Clearfield, A.; Sharma, C.V.K. and Zhang, B. Crystal Engineered Supramolecular MetalPhosphonates: Crown Ethers and Iminodiacetates. // Chem. Mater. 2001, 13, 3099-3112.105.Evans, O.R.; Manke, D.R. and Lin, W. Homochiral Metal−Organic Frameworks Based onTransition Metal Bisphosphonates.
// Chem. Mater. 2002, 14, 3866-3874.106.Ayyappan, P.; Evans, O.R.; Cui, Y.; Wheeler, K.A. and Lin, W. Nonlinear Optically ActivePolymeric Coordination Networks Based on Metal m-Pyridylphosphonates. // Inorg. Chem.2002, 41, 4978-4980.107.Petrakis, K.S. and Nagabhushan, T.L.
Palladium-catalyzed substitutions of triflates derivedfromtyrosine-containingpeptidesandsimplerhydroxyarenesforming4-(diethoxyphosphinyl)phenylalanines and diethyl arylphosphonates. // J. Am. Chem. Soc. 1987,109, 2831-2833.144108.Enakieva, Y.Y.; Bessmertnykh, A.G.; Gorbunova, Y.G.; Stern, C.; Rousselin, Y.; Tsivadze,A.Y.
and Guilard, R. Synthesis of meso-Polyphosphorylporphyrins and Example of SelfAssembling. // Org. Lett. 2009, 11, 3842-3845.109.Johansson, T. and Stawinski, J. Synthesis of dinucleoside pyridylphosphonates involvingpalladium(0)-catalyzed phosphorus-carbon bond formation as a key step. // Chem. Commun.(Cambridge, U.
