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For aerobic oxidation of alcohols involving formal coupled electron transfer see: a) I. E. Markó, P. R. Giles, M. Tsukazaki, S. M. Brown, C. J. Urch, Science 1996, 274, 2044; b) I. E. Markó, P. R. Giles, M. Tsukazaki, I. Chellé-Regnaut, A. Gautier, S. M. Brown, C. J. Urch, J. Org. Chem. 1999, 64, 2433.
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39
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Apart from those reported in references [22-27] a few noncatalytic methods are known. See for example: K. C. Nicolaou, C. J. N. Mathiason, T. Montagnon, Angew. Chem. 2003. 115, 4111; Angew. Chem. Int. Ed. 2003, 42, 4077. and references therein.
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40
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0141649624
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and references therein
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Apart from those reported in references [22-27] a few noncatalytic methods are known. See for example: K. C. Nicolaou, C. J. N. Mathiason, T. Montagnon, Angew. Chem. 2003. 115, 4111; Angew. Chem. Int. Ed. 2003, 42, 4077. and references therein.
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Murahashi, S.I.1
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44
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17444373399
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note
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For an example of ruthenium-catalyzed aerobic oxidative cyanation see reference [15b].
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45
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A. H. Éll, J. S. M. Samec, C. Brasse, J.-E. Bäckvall, Chem. Commun. 2002, 1144.
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a) K. Yamaguchi, N. Mizuno, Angew. Chem. 2003, 115, 1518: Angew. Chem. Int. Ed. 2003, 42, 1480;
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48
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C. P. Casey, S. W. Singer, D. R. Powell, R. K. Hayashi, M. Kavana, J. Am. Chem. Soc. 2001, 723, 1090.
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54
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17444390387
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note
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v=O that subsequently oxidizes the substrate.
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-
-
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55
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17444371954
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note
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It was shown that 3 and 27 alone (without quinone 2a) slowly catalyzed the aerobic oxidation of amines to imines. After 1 h, <10% conversion to imine was observed compared to > 30% with the coupled system. However no oxidation took place without 3 (reaction checked after 4 h).
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59
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0035817667
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+ at the proton/ammonium position see: H. M. Jung, S. T. Shin, Y. H. Kim, M.-J. Kim, J. Park, Organometallics 2001, 20, 3370.
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Brigaud, T.7
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63
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17444419310
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note
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Air with toluene at 100°C produces explosive mixtures in the gas phase.
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