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0037006847
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c) H. D. Bendorf, C. M. Colella, E. C. Dixon, M. Marchetti, A. N. Matukonis, J. D. Musselman, T. A. Tiley, Tetrahedron Lett. 2002, 45, 7031.
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For selected examples, see: a) T. B. Marder, D. C. Roe, D. Milstein, Organometallics 1988, 7, 1451;
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b) T. Kondo, N. Hiraishi, Y. Morisaki, K. Wada, Y. Watanabe, T.-a. Mitsudo, Organometallics 1998, 17, 2131;
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c) C. P. Lenges, P. S. White, M. J. Brookhart, J. Am. Chem. Soc. 1998, 120, 6965;
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a) M. C. Willis, S. J. McNally, P. J. Beswick, Angew. Chem. Int. Ed. 2004, 43, 340;
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23
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33845233052
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note
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2 (Ref. [4a]) can be isolated, it is relatively air sensitive, and in our hands its use led to variable results.
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-
-
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33
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33845231034
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note
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4) was also active, although the reaction required 4 h to reach completion.
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-
-
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34
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33845201872
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note
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The product from entry 4 (Table 2) was obtained in 33 % yield with the original catalyst. See Ref. [7a].
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35
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0037185310
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S.-M. Kuang, P. E. Fanwick, R. A. Wallon, Inorg. Chem. 2002, 41, 405.
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0001182381
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b) C. Bianchini, A. Meili, M. Peruzzini, F. Vizza, F. Bachechi, Organometallics 1991, 10, 820;
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Bianchini, C.1
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0001228257
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c) K. Wang, T. J. Emge, A. S. Goldman, C. Li, S. P. Nolan, Organometallics 1995, 14, 4929;
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42
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37049091603
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For an example of a spectroscopically characterized acyl-hydrido species that undergoes intramolecular hydroacylation, see: D. Milstein, J. Chem. Soc. Chem. Commun. 1982, 1357.
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Milstein, D.1
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