Диссертация (1150329), страница 14
Текст из файла (страница 14)
− V. 3. − N 6. − P.546–553.10380. Carril, M. Palladium and copper-catalysed arylation reactions in the presenceof water, with a focus on carbon–heteroatom bond formation / M. Carril, R.SanMartin, E. Domınguez // Chem. Soc. Rev. − 2008. − V. 37. − N 4. − P.639−647.81.
Zhu, X. Bis(cyclohexanone) oxalyldihydrazone/copper(ii) oxide - a novel andefficient catalytic system for Ullmann-type C-N coupling in pure water /X.Zhu, Y. Ma, L. Su, H. Song, G. Chen, D. Liang, Y. Wan // Synthesis. − 2006.− V. 23. − P. 3955−3962.82. Zhu, X. A Facile and efficient oxalyldihydrazide/ketone-promoted coppercatalyzed amination of aryl halides in water / X.
Zhu, L. Su, L. Huang, G.Chen, J. Wang, H. Song, Y. Wan // Eur. J. Org. Chem. − 2009. − V. 2009. − N5. − P. 635–642.83. Xie, J. Pyrrole-2-carbohydrazides as ligands for Cu-catalyzed amination of arylhalides with amines in pure water / J. Xie, X. Zhu, M. Huang, F. Meng, W.Chen, Y. Wan // Eur. J. Org. Chem. − 2010. − V. 2010. – N 17.− P.3219−3223.84. Sperotto, E.
The mechanism of the modified Ullmann reaction / E. Sperotto,G.Van Klink, G.Van Koten, J. De Vries // Dalton Trans. − 2010. − V. 39. − N43.− P. 10338−10351.85. Casitas, A. Direct observation of CuI/CuIII redox steps relevant to Ullmanntype coupling reactions / A. Casitas, A.
King, T. Parella, M. Costas, S. Stahl,X. Ribas // Chemical Science. − 2010. − V. 1. − N 3.− P. 326−330.86. Paine, A. Mechanisms and models for copper mediated nucleophilic aromaticsubstitution. 2. Single catalytic species from three different oxidation states ofcopper in an Ullmann synthesis of triarylamines / A. Paine // J. Am. Chem.Soc. − 1987.− V. 109.
– N 5. − P. 1496–1502.87. Roy, A. Directly observed reductive elimination of aryl halides frommonomeric arylpalladium(II) halide complexes / A. Roy, J. Hartwig // J. Am.Chem. Soc. − 2003. − V. 125. – N 46.− P. 13944−13945.10488. Stambuli, J. Synthesis, characterization, and reactivity of monomeric,arylpalladium halide complexes with a hindered phosphine as the only dativeligand / J.
Stambuli, M. Bühl, J. Hartwig, // J. Am. Chem. Soc. − 2002. − V.124. − N 32.− P. 9346−9347.89. Casado, A. Mechanism of the Stille reaction. 1. The transmetalation step.Coupling of R1I and R2SnBu3 catalyzed by trans-[PdR1IL2] (R1 = C6Cl2F3; R2 =Vinyl, 4-Methoxyphenyl; L = AsPh3) / A. Casado, P. Espinet // J. Am. Chem.Soc. − 1998. − V. 120. − N 35.− P. 8978−8985.90. Casado, A. On the configuration resulting from oxidative addition of RX toPd(PPh3)4 and the mechanism of the cis-to-trans isomerization of[PdRX(PPh3)2] complexes (R = Aryl, X = Halide)/ A.
Casado, P. Espinet //Organometallics. − 1998. − V. 17. − N 5.− P. 954−959.91. Amatore, C. Anionic Pd(0) and Pd(II) intermediates in palladium-catalyzedHeck and cross-coupling reactions / C. Amatore, A. Jutand // Acc. Chem. Res.− 2000. − V. 33. – N 5.− P. 314−321.92. Amatore, C. Rates and mechanism of the reversible oxidative addition of (Z)and (E)-1,2-dichloroethylene to low-ligated zerovalent palladium / C.
Amatore,M. Azzabi, A. Jutand // J. Am. Chem. Soc. − 1991. − V. 113. – N 5.− P.1670−1677.93. Bickelhaupt, F. Oxidative insertion as frontside SN2 substitution: a theoreticalstudy of the model reaction system Pd + CH3Cl / F. Bickelhaupt, T. Ziegler, P.Schleyer // Organometallics. − 1995. − V. 14. – N 5.− P.
2288−2296.94. Diefenbach, A. Oxidative addition of Pd to C–H, C–C and C–Cl bonds:importance of relativistic effects in DFT calculations / A. Diefenbach, F.Bickelhaupt // J. Chem. Phys. − 2001. − V. 115. – N 9.− P. 4030−4040.95. Albert, K. On C−C coupling by carbene-stabilized palladium catalysts: adensity functional study of the Heck reaction / K. Albert, P. Gisdakis, N. Rösch// Organometallics. − 1998.− V.
17. – N 8.− P.1608−1616.10596. Sundermann, A. Computational study of a new Heck reaction mechanismcatalyzed by palladium (II/IV) species / A. Sundermann, O. Uzan, J. Martin //Chem. – Eur. J. − 2001. V. 7. – N 8.− P. 1703−1711.97. Senn, H. Oxidative addition of aryl halides to palladium (0) complexes: adensity-functional study including solvation / H. Senn, T. Ziegler //Organometallics. − 2004.− V.
23. − N 12. − P. 2980−2988.98.Crabtree, R. The Organometallic Chemistry of the Transition Metals / R.Crabtree. − New Jersey: John Wiley − Interscience John Wiley & Sons, Inc.,Hoboken, 2005.99. Uhlig, E. Synthesis with electron-rich nickel triad complexes/ E. Uhlig, D.Waton // Coord. Chem. Rev. − 1980. − V. 33. − N 1. − P. 3−53.100. Thomas, C. Ligand effects in the rhodium-catalyzed carbonylation of methanol/ C. Tomas, G. Suss-Fink // Coord. Chem. Rev. − 2003. − V. 243. − N 1−2.
−P. 125−142.101. Stille, J. Mechanisms of oxidative addition of organic halides to Group 8transition-metal complexes / J. Stille, K. Lau // Acc. Chem. Res. − 1977. − V.10. − N 12. − P. 434−442.102. Kim, J. Evidence for a radical mechanism of aromatic "nucleophilic"substitution / J. Kim, J. Bennett // J. Am. Chem. Soc. − 1970. − V. 92. − N 25.− P. 7463−7464.103. Кузьмин М.Г. Ион-радикальные цепные реакции. Неклассические цепныереакции, протекающие через стадию переноса электрона / М.Г. Кузьмин,А.Е.
Шилов // Химическая физика на пороге XXI века. К 100-летию акад.Н.Н. Семенова. 1996, Москва, с. 21‒36.104. Borosky, G. Differences in reactivity of stabilized carbanions with haloarenesin the initiation and propagation steps of the SRN1 mechanism in DMSO / G.Borosky, A. Pierini, R. Rossi // J. Org. Chem. − 1992. − V. 57. − N 1. − P.247–252.106105. Saveant, J.-M. Catalysis of chemical reactions by electrodes / J.-M. Saveant //Acc.
Chem. Res. − 1980. − V. 13. N 9. − P. 323–329106. Росcи Р.А. Ароматическое замещение по SRN1 механизму: Пер. с англ. /Р.А. Росси, Р.Х. де Росси – М.: Мир, 1986.107. Noell, J. Oxidative addition of hydrogen to bis(phosphine)platinum(0)complexes: an ab initio theoretical treatment / J. Noell, P. Hay // J. Am. Chem.Soc. − 1982. − V. 104. − N 17.
− P. 4578–4584.108. Low, J. Theoretical studies of oxidative addition and reductive elimination: H2+ Pt(PH3)2 → Pt(H)2(PH3)2 / J. Low, W. Goddard // J. Am. Chem. Soc. −1984.− V. 106. − N 23. − P. 6928–6937.109. Obara, S. Reaction mechanisms of oxidative addition [H2 + Pt0(PH3)2 →PtΙΙ(H)2(PH3)2] and reductive elimination v PtΙΙ(H)(CH3)(PH3)2 → CH4 +PtΙΙ(PH3)2.
Ab initio MO study / S. Obara, K. Kitaura, K. Morokuma // J. Am.Chem. – 1984. – V. 106. – N 24. – P. 7482−7492.110. Ahlquist, M. Oxidative addition of aryl chlorides to monoligated palladium(0): a DFT-SCRF study / A. Ahlquist, P-A. Norrby // Organometallics. − 2007. −V.
26. − N 3. − P. 550–553.111. Li, Z. Theoretical study on monoligated Pd-catalyzed cross-coupling reactionsof aryl chlorides and bromides / Z. Li, Y. Fu, Q.-X. Guo, L. Liu //Organometallics. − 2008. − V. 27. − N 16. − P. 4043–4049.112. Jover, J. A computational study of phosphine ligand effects in Suzuki–Miyauracoupling / J. Jover, J. Harvey, N. Fey, M. Purdie, G. Lloyd-Jones, J. // J. Mol.Catal. A: Chem.− 2010.
− V. 324.− N 1−2. − P. 39−47.113. Schoenebeck, F. Ligand-controlled regioselectivity in palladium-catalyzedcross coupling reactions / F. Schoenebeck, N. Houkk // J. Am. Chem. Soc. −2010.− V. 132. − N 8. − P. 2496–2497.114. Casado, A. Mechanism of the Stille Reaction. The Transmetalation Step.Coupling of R1I and R2SnBu3 Catalyzed by trans-[PdR1IL2] (R1 = C6Cl2F3; R2107= Vinyl, 4-Methoxyphenyl; L = AsPh3) // J. Am. Chem.
Soc. − 1998.− V. 120.− P. 8978−8985.115. Casado, A. On the Configuration Resulting from Oxidative Addition of RX toPd(PPh3)4 and the Mechanism of the cis-to-trans Isomerization of[PdRX(PPh3)2] Complexes (R = Aryl, X = Halide) / A. Casado, P.Espinet //Organometallics. – 1998. – V. 17. – N 5. – P. 954-959.116. Fitton, P.
Oxidative additions to palladium(0) / P. Fitton, M. Johnson, J.McKeon // Chem. Commun. − 1968. − P. 6−7.117. Amatore, C. Intimate mechanism of oxidative addition to zerovalent palladiumcomplexes in the presence of halide ions and its relevance to the mechanism ofpalladium-catalyzed nucleophilic substitutions / C. Amatore, A. Jutand, A.Suarez // J. Am. Chem. Soc. − 1993.
– V. 115. − N 21. − P. 9531–9541.118. Amatore, C. Mechanism of oxidative addition of palladium(0) with aromaticiodides in toluene, monitored at ultramicroelectrodes / C. Amatore, F. Pflüger// Organometallics. − 1990. – V. 9. − N 8. − P. 2276−2282.119. Amatore, C. A. Rates and mechanism of the reversible oxidative addition of(Z)- and (E)-1,2-dichloroethylene to low-ligated zerovalent palladium / C.Amatore, M.
Azzabi, A. Jutand // J. Am. Chem. Soc. − 1991. – V. 113. − N 5.− P. 1670–1677.120. Amatore, C. Anionic Pd(0) and Pd(II) Intermediates in Palladium-CatalyzedHeck and Cross-Coupling Reactions / C. Amatore, A. Jutand // Acc. Chem.Res. – 2000. – V. 33. – P. 314–321.121. Hansson, S. Effects of phenanthroline type ligands on the dynamic processes of(η3-allyl)palladium complexes. Molecular structure of (2,9-dimethyl-1,10phenanthroline)[(1,2,3-η)-3-methyl-2-butenyl]chloropalladium / S. Hansson,P.-O. Norrby, M.
Sjögren, B. Åkermark, M. Cucciolito, F. Giordano, A.Vitagliano // Organometallics. – 1993. – V. 12. − N 12. − P. 4940–4948.108122. Bröring, M. A five coordinate PdII complex stable in solution and in the solidstate / M. Bröring, C Brandt // Chem. Commun. – 2003. – V.
17. − N 9. − P.2156−2157.123. Gooßen, L. The mechanism of the oxidative addition of aryl halides to Pdcatalysts: a DFT investigation / L. Gooßen, D. Koley, H. Hermanna, W. Thiel// Chem. Commun. – 2004. – V. 19. – P. 2141–2143.124. Hartwig J. Oxidative addition of aryl bromide after dissociation of phosphinefromatwo-coordinatepalladium(0)complex,bis(tri-o-tolylphosphine)palladium(0) / J. Hartwig, F. Paul // J. Am. Chem. Soc. – 1995.− V. 117. − N 19. − P. 5373−5374.125. Barrios-Landeros F. Effect of ligand steric properties and halide identity on themechanism for oxidative addition of haloarenes to trialkylphosphine pd(0)complexes / F.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
