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Heck, R.F.1
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T.-C. Wu, US patent 5536870, 1996
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Wu, T.-C.1
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0004100638
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Applications of phosphine ligands in homogeneous catalysis: J. Willey and Sons, New York
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Applications of phosphine ligands in homogeneous catalysis: G.W. Parshall, S. Ittel, Homogenous Catalysis, J. Willey and Sons, New York, 1992
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Parshall, G.W.1
Ittel, S.2
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For comprehensive reviews see: M. Regitz, Angew. Chem. Int. Ed. 35 1996 725
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Arduengo III, A.J.1
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0345584452
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The yield of the reaction was lowered significantly when lower (e.g. 1.2 eq.) or higher (e.g. 2 eq.) amounts of base, respectively olefin are used
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The yield of the reaction was lowered significantly when lower (e.g. 1.2 eq.) or higher (e.g. 2 eq.) amounts of base, respectively olefin are used.
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77
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0025999148
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For polar route (cationic mechanism) see
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For polar route (cationic mechanism) see: W. Cabri, I. Candiani, S. DeBernardinis, F. Francalanci, S. Penco, R. Santi, R. J. Org. Chem. 56 1991 5796
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84
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0344290278
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or as source for synthesis of cyclopalladated imine catalysts (R. Reardon, S. Metts, C. Crittendon, P. Daugherity, E.G. Parsons, Organometallics 14 (1995) 3810) or as source for synthesis of cyclopalladated imine catalysts ([15b])
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2 has been employed as precatalyst for the Heck reaction of aryl iodides in superheated water (R. Reardon, S. Metts, C. Crittendon, P. Daugherity, E.G. Parsons, Organometallics 14 (1995) 3810) or as source for synthesis of cyclopalladated imine catalysts ([15b]).
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(1995)
, vol.14
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85
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0028358588
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2 is used mainly as precatalyst for telomerization reaction of dienes
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2 is used mainly as precatalyst for telomerization reaction of dienes: H. Karlheintz, B. Gruber, K.J. Weese, Tetrahedron Lett. 35 1994 4541
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(1994)
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M.I. Zakharkin, V.V. Guseva, D.D. Sulaimankulova, E.A. Petrushkina, Zh. Org. Chem. 23 1987 1654
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Zakharkin, M.I.1
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Sulaimankulova, D.D.3
Petrushkina, E.A.4
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92
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0344290277
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2/DAB-Cy, run 1:97% in 1 h; run 2:91% in 12 h; run 3: 85% in 24 h)
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2/DAB-Cy, run 1:97% in 1 h; run 2:91% in 12 h; run 3: 85% in 24 h).
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