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For asymmetric hydrogenation of α-chloro aromatic ketones with chiral arene-Ru(II) complex 2, see: Ohkuma, T.; Tsutsumi, K.; Utsumi, N.; Arai, N.; Noyori, R.; Murata, K. Org. Lett. 2007, 9, 255-257.
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For asymmetric hydrogenation of α-chloro aromatic ketones with chiral arene-Ru(II) complex 2, see: Ohkuma, T.; Tsutsumi, K.; Utsumi, N.; Arai, N.; Noyori, R.; Murata, K. Org. Lett. 2007, 9, 255-257.
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For asymmetric transfer hydrogenation of α-hydroxyacetophenone, see: a
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For asymmetric transfer hydrogenation of α-hydroxyacetophenone, see: (a) Cross, D. J.; Kenny, J. A.; Houson, I.; Campbell, L.; Walsgrove, T.; Wills, M. Tetrahedron: Asymmetry 2001, 12, 1801-1806.
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2 gave the chiral diol in high ee. See: Morgan, J. B.; Morken, J. P. J. Am. Chem. Soc. 2004, 126, 15338-15339.
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2 gave the chiral diol in high ee. See: Morgan, J. B.; Morken, J. P. J. Am. Chem. Soc. 2004, 126, 15338-15339.
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33947152478
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For asymmetric hydrogenation of arylglyoxal dialkylacetals, see
-
For asymmetric hydrogenation of arylglyoxal dialkylacetals, see: Arai, N.; Ooka, H.; Azuma, K.; Yabuuchi, T.; Kurono, N.; Inoue, T.; Ohkuma, T. Org. Lett. 2007, 9, 939-941.
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0034641294
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For asymmetric hydrogenation of amino ketones catalyzed by chiral Ru complexes, see
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For asymmetric hydrogenation of amino ketones catalyzed by chiral Ru complexes, see: Ohkuma, T.; Ishii, D.; Takeno, H.; Noyori, R. J. Am. Chem. Soc. 2000, 122, 6510-6511.
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28544442793
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See for example
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See for example: Edmonds, J. S.; Morita, M., Turner, P.; Skelton, B. W.; White, A. H. Steroids 2006, 71, 34-41.
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0002588612
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For asymmetric transfer hydrogenation of ketones catalyzed by TsDPEN-Cp*Ir complexes, see: a
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For asymmetric transfer hydrogenation of ketones catalyzed by TsDPEN-Cp*Ir complexes, see: (a) Mashima, K.; Abe, T.; Tani, K. Chem. Lett. 1998, 1199-1200.
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(c) Murata, K.; Ikariya, T.; Noyori, R. J. Org. Chem. 1999, 64, 2186-2187.
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33749516319
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2 gave the IrH species. See: Heiden, Z. M.; Rauchfuss, T. B. J. Am. Chem. Soc. 2006, 128, 13048-13049.
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2 gave the IrH species. See: Heiden, Z. M.; Rauchfuss, T. B. J. Am. Chem. Soc. 2006, 128, 13048-13049.
-
-
-
-
32
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34547155132
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-
Due to the group priority in nomenclature, (R)-4a-j,l and (S)-4k have the same β configuration in Scheme 1.
-
Due to the group priority in nomenclature, (R)-4a-j,l and (S)-4k have the same β configuration in Scheme 1.
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