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Recent reviews on palladium copolymerization catalysts: a
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Recent reviews on palladium copolymerization catalysts: (a) Durand, J.; Milani, B. Coord. Chem. Rev. 2006, 250, 542.
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Coord. Chem. Rev
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Durand, J.1
Milani, B.2
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(c) García Suárez, E. J.; Godard, C.; Ruiz, A.; Claver, C. Eur. J. Inorg. Chem. 2007, 2582.
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Eur. J. Inorg. Chem
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García Suárez, E.J.1
Godard, C.2
Ruiz, A.3
Claver, C.4
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5
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0346182137
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Rieger, B, Ed, Wiley-VCH: Weinheim, Germany
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(b) Consiglio, G. In Late Transition Metal Polymerization Catalysis; Rieger, B., Ed.; Wiley-VCH: Weinheim, Germany, 2003; pp 279-305.
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(2003)
Late Transition Metal Polymerization Catalysis
, pp. 279-305
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Consiglio, G.1
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6
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33749999725
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Recent examples of palladium-methyl catalysts with nitrogen ligands: (a) Durand, J.; Zangrando, E.; Stener, M.; Fronzoni, G.; Carfagna, C.; Binotti, B.; Kamer, P. C. J.; Mueller, C.; Caporali, M.; van Leeuwen, P. W. N. M.; Vogt, D.; Milani, B. Chem. Eur. J. 2006, 12, 7639.
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Recent examples of palladium-methyl catalysts with nitrogen ligands: (a) Durand, J.; Zangrando, E.; Stener, M.; Fronzoni, G.; Carfagna, C.; Binotti, B.; Kamer, P. C. J.; Mueller, C.; Caporali, M.; van Leeuwen, P. W. N. M.; Vogt, D.; Milani, B. Chem. Eur. J. 2006, 12, 7639.
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(b) Schaetz, A.; Scarel, A.; Zangrando, E.; Mosca, L.; Carfagna, C.; Gissibl, A.; Milani, B.; Reiser, O. Organometallics 2006, 25, 4065.
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(2006)
Organometallics
, vol.25
, pp. 4065
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Schaetz, A.1
Scarel, A.2
Zangrando, E.3
Mosca, L.4
Carfagna, C.5
Gissibl, A.6
Milani, B.7
Reiser, O.8
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8
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26844438488
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(c) Scarel, A.; Durand, J.; Franchi, D.; Zangrando, E.; Mestroni, G.; Carfagna, C.; Mosca, L.; Seraglia, R.; Consiglio, G.; Milani, B. Chem. Eur. J. 2005, 11, 6014.
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(2005)
Chem. Eur. J
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Scarel, A.1
Durand, J.2
Franchi, D.3
Zangrando, E.4
Mestroni, G.5
Carfagna, C.6
Mosca, L.7
Seraglia, R.8
Consiglio, G.9
Milani, B.10
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9
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0035977652
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Unexpected 1,2-styrene insertion explains the polymer production of a P - P-based palladium catalyst: Nozaki, K.; Komaki, H.; Kawashima, Y.; Hiyama, T.; Matsubara, T. J. Am. Chem. Soc. 2001, 123, 534.
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Unexpected 1,2-styrene insertion explains the polymer production of a P - P-based palladium catalyst: Nozaki, K.; Komaki, H.; Kawashima, Y.; Hiyama, T.; Matsubara, T. J. Am. Chem. Soc. 2001, 123, 534.
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10
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2] catalysts: (a) Scarel, A.; Milani, B.; Zangrando, E.; Stener, M.; Furlan, S.; Fronzoni, G.; Mestroni, G.; Gladiali, S.; Carfagna, C.; Mosca, L. Organometallics 2004; 23, 1974.
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2] catalysts: (a) Scarel, A.; Milani, B.; Zangrando, E.; Stener, M.; Furlan, S.; Fronzoni, G.; Mestroni, G.; Gladiali, S.; Carfagna, C.; Mosca, L. Organometallics 2004; 23, 1974.
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0000139707
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(b) Milani, B.; Scarel, A.; Mestroni, G.; Gladiali, S.; Taras, R.; Carfagna, C.; Mosca, L. Organometallics 2002, 21, 1323.
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(2002)
Organometallics
, vol.21
, pp. 1323
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Milani, B.1
Scarel, A.2
Mestroni, G.3
Gladiali, S.4
Taras, R.5
Carfagna, C.6
Mosca, L.7
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0034245677
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(c) Milani, B.; Corso, G.; Mestroni, G.; Carfagna, C.; Formica, M.; Seraglia, R. Organometallics 2000, 19, 3435.
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(2000)
Organometallics
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Milani, B.1
Corso, G.2
Mestroni, G.3
Carfagna, C.4
Formica, M.5
Seraglia, R.6
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13
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4243201387
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Electronic effects can be crucial in this process: (a) Reference 3a. (b) Bastero, A.; Ruiz, A.; Claver, C.; Castillón, S.; Daura, E.; Bo, C.; Zangrando, E. Chem. Eur. J. 2004, 10, 3747.
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Electronic effects can be crucial in this process: (a) Reference 3a. (b) Bastero, A.; Ruiz, A.; Claver, C.; Castillón, S.; Daura, E.; Bo, C.; Zangrando, E. Chem. Eur. J. 2004, 10, 3747.
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0034679517
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(c) Gambs, C.; Chaloupka, S.; Consiglio, G.; Togni, A. Angew. Chem., Int. Ed. 2000, 39, 2486.
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(2000)
Angew. Chem., Int. Ed
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, pp. 2486
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Gambs, C.1
Chaloupka, S.2
Consiglio, G.3
Togni, A.4
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15
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37049076733
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(a) Amouyal, E.; Homsi, A.; Chambron, J. C.; Sauvage, J. P. J. Chem. Soc., Dalton Trans. 1990, 1841.
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(1990)
J. Chem. Soc., Dalton Trans
, pp. 1841
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Amouyal, E.1
Homsi, A.2
Chambron, J.C.3
Sauvage, J.P.4
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16
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0030605860
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(b) López, R.; Loeb, B.; Bossie, T.; Meyer, T. J. Tetrahedron Lett. 1996, 37, 5437.
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(1996)
Tetrahedron Lett
, vol.37
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López, R.1
Loeb, B.2
Bossie, T.3
Meyer, T.J.4
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17
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0035759419
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(c) Arancibia, A.; Concepción, J.; Daire, N.; Leiva, G.; Leiva, A. M.; Loeb, B.; del Rio, R.; Díaz, R.; Francois, A.; Valdivia, M. J. Coord. Chem. 2001, 54, 323.
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J. Coord. Chem
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Arancibia, A.1
Concepción, J.2
Daire, N.3
Leiva, G.4
Leiva, A.M.5
Loeb, B.6
del Rio, R.7
Díaz, R.8
Francois, A.9
Valdivia, M.10
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18
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41749110602
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Phenanthroline (phen) and phen derivatives have shown superior performance as ligands in this reaction.3a,5
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3a,5
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19
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41749102077
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See ref 2a, in particular Chapter 4, p 110 by Mul, W. P.; van der Made, A. W.; Smaardijk, A. A., Drent, E.
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See ref 2a, in particular Chapter 4, p 110 by Mul, W. P.; van der Made, A. W.; Smaardijk, A. A., Drent, E.
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0037224622
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Aguirre, P.; López, R.; Villagra, D.; Azocar-Guzman, I.; Pardey, A. J.; Moya, S. A. Appl. Organomet. Chem. 2003, 17, 36-41.
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(2003)
Appl. Organomet. Chem
, vol.17
, pp. 36-41
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Aguirre, P.1
López, R.2
Villagra, D.3
Azocar-Guzman, I.4
Pardey, A.J.5
Moya, S.A.6
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21
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33846354160
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Bergman, S. D.; Goldberg, I.; Carfagna, C.; Mosca, L.; Kol, M.; Milani, B. Organometallics 2006, 25, 6014.
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(2006)
Organometallics
, vol.25
, pp. 6014
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Bergman, S.D.1
Goldberg, I.2
Carfagna, C.3
Mosca, L.4
Kol, M.5
Milani, B.6
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22
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0001447529
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Brookhart, M.; Rix, F. C.; DeSimone, J. M. J. Am. Chem. Soc. 1992, 114, 5894.
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(1992)
J. Am. Chem. Soc
, vol.114
, pp. 5894
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Brookhart, M.1
Rix, F.C.2
DeSimone, J.M.3
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23
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NMR spectra were not informative, due to the low solubility of the products
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NMR spectra were not informative, due to the low solubility of the products.
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24
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41749102308
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13C spectra, except for 2a.
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13C spectra, except for 2a.
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25
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33947715682
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Such mixtures of geometric isomers have reported for similar palladium-methyl complexes: (a) Leone, A.; Gischig, S.; Elsevier, C. J.; Consiglio, G. J. Organomet. Chem. 2007, 692, 2056.
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Such mixtures of geometric isomers have reported for similar palladium-methyl complexes: (a) Leone, A.; Gischig, S.; Elsevier, C. J.; Consiglio, G. J. Organomet. Chem. 2007, 692, 2056.
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1842767168
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Reference 3b. (c) Soro, B.; Stoccoro, S.; Cinellu, M. A.; Minghetti, G.; Zueca, A.; Bastero, A.; Claver, C. J. Organomet. Chem. 2004, 689, 1521.
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(b) Reference 3b. (c) Soro, B.; Stoccoro, S.; Cinellu, M. A.; Minghetti, G.; Zueca, A.; Bastero, A.; Claver, C. J. Organomet. Chem. 2004, 689, 1521.
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tert-Butylstyrene instead of styrene is used to afford soluble alt-CO-tert-butylstyrene polyketones: Brookhart, M, Rix, F. C, DeSimone, J. M. J. Am. Chem. Soc. 1992, 114, 5895-5897
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tert-Butylstyrene instead of styrene is used to afford soluble alt-CO-tert-butylstyrene polyketones: Brookhart, M.; Rix, F. C.; DeSimone, J. M. J. Am. Chem. Soc. 1992, 114, 5895-5897.
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Hansch, C.; Leo, A.; Taft, R. W. Chem. Rev. 1991, 91, 165-195.
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(1991)
Chem. Rev
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, pp. 165-195
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Hansch, C.1
Leo, A.2
Taft, R.W.3
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Although activity measurements should be performed to state this point, the absence of black palladium at the end of the reaction seems to indicate the higher stability of these catalysts
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Although activity measurements should be performed to state this point, the absence of black palladium at the end of the reaction seems to indicate the higher stability of these catalysts.
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