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For recent reviews, see: (a) B. Cornus, Angew. Chem., Int. Ed. Eng., 1997, 36, 2057;
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13
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0030565451
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For recent examples of the oxidation using FBS, see: (a) G. Pozzi, S. Banfi, A. Manfredi, F. Montanari and S. Quici, Tetrahedron, 1996, 52, 11879;
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For recent examples of the oxidation using molecular oxygen in FBS, see: (a) S. G. DiMagno, P. H. Dussault and J. A. Schultz, J. Am. Chem. Soc., 1996, 118, 5312;
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(e) G. Pozzi, M. Cavazzini, S. Quici and S. Fontana, Tetrahedron Lett., 1997, 38, 7605;
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(f) G. Pozzi, F. Cinato, F. Montanari and S. Quici, Chem. Commun., 1998, 877;
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0034051594
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(b) M. Besson and P. Callezot, Catal. Today, 2000, 57, 127 and references cited therein.
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For examples of the aerobic oxidation of alcohols in fluorinated organic solvents, see: (a) A. Hanyu, E. Takezawa, S. Sakaguchi and Y. Ishii, Tetrahedron Lett., 1998, 38, 5557;
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36
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33645923292
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note
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We also tried to optimize the reaction conditions, such as temperature, solvents and additives, for the homogeneous reaction, but the optimum conditions could not be found because of the formation of a palladium black in the homogeneous phase reaction.
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-
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37
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33645927505
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2 as well as water partly formed by its decomposition; ref. 9(b)
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2 as well as water partly formed by its decomposition; ref. 9(b).
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38
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33645916581
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We succeeded in the oxidation of allylic alcohols in our previous reported catalytic systems; refs. 9(b) and 10
-
We succeeded in the oxidation of allylic alcohols in our previous reported catalytic systems; refs. 9(b) and 10.
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-
-
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39
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33645918159
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note
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In several trials of the reaction using the recycled fluorous phase without the addition of a ligand, the precipitation of a palladium black was sometimes observed and the yield decreased. On the other hand, when further ligand was added for each run, the yield of the product gradually decreased, because a large excess of ligand lowered the reaction rate.
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