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Reviews:
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Reviews:
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0037112673
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A. F. Littke, G. C. Fu, Angew. Chem. 2002, 114, 4350-4386; Angew. Chem. Int. Ed. 2002, 41, 4176-4211;
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Frisch, A.C.1
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7
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For example:
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For example:
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0034680642
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A. Zapf, A. Ehrentraut, M. Beller, Angew. Chem. 2000, 112, 4315-4317; Angew. Chem. Int. Ed. 2000, 39, 4153-4155;
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C. Amatore, A. Jutand, G. Meyer, H. Atmani, F. Khalil, F. O. Chahdi, Organometallics 1998, 17, 2958-2964;
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Amatore, C.1
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19
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R. Kreiter, R. J. M. Klein Gebbink, G. van Koten, Tetrahedron 2003, 59, 3989-3997.
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D. J. M. Snelders, R. Kreiter, J. J. Firet, G. van Koten, R. J. M. Klein Gebbink, Adv. Synth. Catal. 2008, 350, 262-266;
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Snelders, D.J.M.1
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21
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68849102223
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D. J. M. Snelders, G. van Koten, R. J. M. Klein Gebbink, J. Am. Chem. Soc. 2009, 131, 11407-11416.
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Snelders, D.J.M.1
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14844328047
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R. B. De Vasher, J. M. Spruell, D. A. Dixon, G. A. Broker, S. T. Griffin, R. D. Rogers, K. H. Shaughnessy, Organometallics 2005, 24, 962-971;
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23
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L. R. Moore, E. C. Western, R. Craciun, J. M. Spruell, D. A. Dixon, K. P. O'Halloran, K. H. Shaughnessy, Organometallics 2008, 27, 576-593.
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25
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R. Kreiter, J. J. Firet, M. J. J. Ruts, M. Lutz, A. L. Spek, R. J. M. Klein Gebbink, G. van Koten, J. Organomet. Chem. 2006, 691, 422-432.
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29
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0001124770
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T. Bartik, B. Bartik, B. E. Hanson, I. Guo, I. Toth, Organometallics 1993, 12, 164-170.
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Bartik, T.1
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79957677236
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2] complex was observed as a minor product at 34.3ppm.
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2] complex was observed as a minor product at 34.3ppm.
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31
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79957776990
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0 is assumed to be very rapid under catalytic conditions.
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0 is assumed to be very rapid under catalytic conditions.
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32
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79957756715
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Traces of oxygen that can still be present in the solvent, could possibly serve as the oxidant.
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Traces of oxygen that can still be present in the solvent, could possibly serve as the oxidant.
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33
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The structure of this species is unknown. It may be dimeric, or contain a halide ion or a solvent molecule as additional ligand.
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The structure of this species is unknown. It may be dimeric, or contain a halide ion or a solvent molecule as additional ligand.
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35
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33748659720
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C. Palau, Y. Berchadsky, F. Chalier, J. Finet, G. Gronchi, P. J. Tordo, J. Phys. Chem. 1995, 99, 158-163.
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A. S. Howell, N. Fey, J. D. Lovatt, P. C. Yates, P. McArdle, D. Cunningham, E. Sadeh, H. E. Gottlieb, Z. Goldschmidt, M. B. Hursthouse, M. E. Light, J. Chem. Soc. Dalton Trans. 1999, 3015-3028;
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sted., Longman, London 1987, p.137.
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Isaacs, N.S.1
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45
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79957714181
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The Weak Hydrogen Bond in Structural Chemistry and Biology
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51
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[26] maximum semicone angles for 1a were determined from the crystal structure of 1a(S) to be 70°, 102°, and 107°, leading to an average Tolman cone angle of 186°.
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[26] maximum semicone angles for 1a were determined from the crystal structure of 1a(S) to be 70°, 102°, and 107°, leading to an average Tolman cone angle of 186°.
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56
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18844392282
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Lam, K.C.1
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61
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3, 7b, and 7c, the higher activity at a lower Pd loading is most likely a question of entropy. As the forward reactions of equilibria1 and2 lead to an increase in the total number of species, a lower concentration is expected to shift these equilibria forwards, that is, to the side of the coordinatively unsaturated, active species.
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3, 7b, and 7c, the higher activity at a lower Pd loading is most likely a question of entropy. As the forward reactions of equilibria1 and2 lead to an increase in the total number of species, a lower concentration is expected to shift these equilibria forwards, that is, to the side of the coordinatively unsaturated, active species.
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63
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