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1
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84871014549
-
-
For reviews and accounts on this catalytic transformation, see
-
For reviews and accounts on this catalytic transformation, see
-
-
-
-
9
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84871001634
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-
For mechanistic studies, see
-
For mechanistic studies, see
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13
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See, for example
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See, for example
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P. Servin, R. Laurent, L. Gonsalvi, M. Tristany, M. Peruzzini, J.-P. Majoral, and A.-M. Caminade Dalton Trans. 2009 4432 4434
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P. Servin, R. Laurent, H. Dib, L. Gonsalvi, M. Peruzzini, J.-P. Majoral, and A.-M. Caminade Tetrahedron Lett. 53 2012 3876 3879
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39
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84870993066
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2 atmosphere
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2 atmosphere
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44
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78651352697
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S.E. García-Garrido, J. Francos, V. Cadierno, J.-M. Basset, and V. Polshettiwar ChemSusChem 4 2011 104 111
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Martín-Matute, B.7
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46
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0141750679
-
-
2, showing only a modest catalytic activity, have also been described
-
2, showing only a modest catalytic activity, have also been described: C.M. Standfest-Hauser, T. Lummerstorfer, R. Schmid, K. Kirchner, H. Hoffmann, and M. Puchberger Monatsh. Chem. 134 2003 1167 1175
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Schmid, R.3
Kirchner, K.4
Hoffmann, H.5
Puchberger, M.6
-
47
-
-
53849145021
-
-
3 was also employed as a recyclable system in the reduction of allylic alcohols through a tandem redox isomerization/transfer hydrogenation reaction
-
3 was also employed as a recyclable system in the reduction of allylic alcohols through a tandem redox isomerization/transfer hydrogenation reaction: J.W. Kim, T. Koike, M. Kotani, Y. Yamaguchi, and N. Mizuno Chem. Eur. J. 14 2008 4104 4109
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Kim, J.W.1
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Mizuno, N.5
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48
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84870987636
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For representative recent examples, see
-
For representative recent examples, see
-
-
-
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50
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84861527044
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A. Romero-Pérez, A. Infantes-Molina, A. Jiménez- López, E.R. Jalil, K. Sapag, and E. Rodríguez-Castellón Catal. Today 187 2012 88 96
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Sapag, K.5
Rodríguez-Castellón, E.6
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54
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84870986819
-
-
For reviews on the coordination chemistry of the PTA ligand (1,3,5-triaza-7-phosphaadamantane) and its derivatives, see
-
For reviews on the coordination chemistry of the PTA ligand (1,3,5-triaza-7-phosphaadamantane) and its derivatives, see
-
-
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55
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4544321309
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A.D. Phillips, L. Gonsalvi, A. Romerosa, F. Vizza, and M. Peruzzini Coord. Chem. Rev. 248 2004 955 993
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A. Briot, C. Baehr, R. Brouillard, A. Wagner, and C. Mioskowski J. Org. Chem. 69 2004 1374 1377
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Mioskowski, C.5
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67
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18444387980
-
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6-p-cymene)(PTA-Me)] (3b) has been previously described
-
6-p-cymene)(PTA-Me)] (3b) has been previously described: A. Dorcier, P.J. Dyson, C. Gossens, U. Rothlisberger, R. Scopelliti, and I. Tavernelli Organometallics 24 2005 2114 2123
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(2005)
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Tavernelli, I.6
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68
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84871009289
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-
Although rare, N-coordination of PTA-based ligands to transition-metals has been documented. See Ref. [20] and works cited therein.
-
Although rare, N-coordination of PTA-based ligands to transition-metals has been documented. See Ref. [20] and works cited therein.
-
-
-
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70
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84870979608
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See, for example
-
See, for example
-
-
-
-
73
-
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0013326691
-
-
The Hg(0)-poisoning test is the most direct method to distinguishing homogeneous from heterogeneous catalysis when transition metals able to form an amalgam are employed. See, for example: and references therein
-
The Hg(0)-poisoning test is the most direct method to distinguishing homogeneous from heterogeneous catalysis when transition metals able to form an amalgam are employed. See, for example: J.A. Widegren, and R.G. Finke J. Mol. Catal. A: Chem. 198 2003 317 341 and references therein
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Widegren, J.A.1
Finke, R.G.2
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74
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77955690460
-
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6-arene)(NHC)][Cs] (NHC = N-heterocyclic carbene ligand) have been described by Peris and co-workers as active catalysts for the redox isomerization of allylic alcohols
-
6-arene)(NHC)][Cs] (NHC = N-heterocyclic carbene ligand) have been described by Peris and co-workers as active catalysts for the redox isomerization of allylic alcohols: A. Azua, S. Sanz, and E. Peris Organometallics 29 2010 3661 3664
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(2010)
Organometallics
, vol.29
, pp. 3661-3664
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Azua, A.1
Sanz, S.2
Peris, E.3
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75
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84871017320
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See, for example, Ref. [2d] and
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See, for example, Ref. [2d] and
-
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76
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26644463231
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Y. Takai, R. Kitaura, E. Nakatami, T. Onishi, and H. Kurosawa Organometallics 24 2005 4729 4733
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(2005)
Organometallics
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Takai, Y.1
Kitaura, R.2
Nakatami, E.3
Onishi, T.4
Kurosawa, H.5
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77
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26844580100
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B. Martín-Matute, K. Bogár, M. Edin, F.B. Kaynak, and J.-E. Bäckvall Chem. Eur. J. 11 2005 5832 5842
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Chem. Eur. J.
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Martín-Matute, B.1
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Edin, M.3
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Bäckvall, J.-E.5
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78
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38049012803
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T. Campos-Malpartida, M. Fekete, F. Joó, Á. Kathó, A. Romerosa, M. Saoud, and W. Wojtków J. Organomet. Chem. 693 2008 468 474
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Campos-Malpartida, T.1
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Romerosa, A.5
Saoud, M.6
Wojtków, W.7
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80
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84870983466
-
-
Previous studies in our group had already pointed out this effect. See, for example, Ref. [11] and
-
Previous studies in our group had already pointed out this effect. See, for example, Ref. [11] and
-
-
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82
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33748280030
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A.E. Díaz-Álvarez, P. Crochet, M. Zablocka, C. Duhayon, V. Cadierno, J. Gimeno, and J.P. Majoral Adv. Synth. Catal. 348 2006 1671 1679
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Díaz-Álvarez, A.E.1
Crochet, P.2
Zablocka, M.3
Duhayon, C.4
Cadierno, V.5
Gimeno, J.6
Majoral, J.P.7
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84
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71549139771
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V. Cadierno, P. Crochet, J. Francos, S.E. García-Garrido, J. Gimeno, and N. Nebra Green Chem. 11 2009 1992 2000
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Cadierno, V.1
Crochet, P.2
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Nebra, N.6
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86
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84871023758
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See, for example
-
See, for example
-
-
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91
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0042671140
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E. Mas-Marzá, A.M. Segarra, C. Claver, E. Peris, and E. Fernández Tetrahedron Lett. 44 2003 6595 6599
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Segarra, A.M.2
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92
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M. Poyatos, F. Márquez, E. Peris, C. Claver, and E. Fernández New J. Chem. 27 2003 425 431
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Poyatos, M.1
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Fernández, E.5
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94
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84870999285
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-
This was estimated by considering that the totality of complex 3a, including both the organometallic cation and the chloride anion, has been incorporated into the clay and that the totality of the anions and cations present initially in the Montmorillonite-K10 is maintained. It is also assumed that no molecules of solvent have been incorporated in the solid.
-
This was estimated by considering that the totality of complex 3a, including both the organometallic cation and the chloride anion, has been incorporated into the clay and that the totality of the anions and cations present initially in the Montmorillonite-K10 is maintained. It is also assumed that no molecules of solvent have been incorporated in the solid.
-
-
-
-
95
-
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84871001813
-
-
For related examples of superficial adsorption of ionic organometallic complexes in Montmorillonite, see
-
For related examples of superficial adsorption of ionic organometallic complexes in Montmorillonite, see
-
-
-
-
98
-
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57249084550
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C. Claver, E. Fernández, R. Margalef-Català, F. Medina, P. Salagre, and J.E. Sueiras J. Catal. 201 2001 70 79
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J. Catal.
, vol.201
, pp. 70-79
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Claver, C.1
Fernández, E.2
Margalef-Català, R.3
Medina, F.4
Salagre, P.5
Sueiras, J.E.6
-
100
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84870984020
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-
Inclusion of a bulky organometallic cation into the layers of Montmorillonite results in an increase of several armstrong of the interlaminar distance of the solid. Examples can be found in Refs. [19,39].
-
Inclusion of a bulky organometallic cation into the layers of Montmorillonite results in an increase of several armstrong of the interlaminar distance of the solid. Examples can be found in Refs. [19,39].
-
-
-
-
101
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84871013127
-
-
We decided to increase the amount of solid employed to minimize mechanical losses of the catalyst during the processes of filtration and washing, as well as in the taking of aliquots for the reaction monitoring by GC.
-
We decided to increase the amount of solid employed to minimize mechanical losses of the catalyst during the processes of filtration and washing, as well as in the taking of aliquots for the reaction monitoring by GC.
-
-
-
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