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Resolution of acetates with lipases and esterases: C. J. Sih, S.-H. Wu, Top. Stereochem. 1989, 19, 63-125; A. M. Klibanov, Acc. Chem. Res. 1990, 23, 114-120; R. Csuk, B. I. Glänzer, Chem. Rev. 1991, 91, 49-97; C. H. Wong, G. M. Whitesides, Enzymes in Synthetic Organic Chemistry; Pergamon, Oxford, 1994: E. Schoffers, A. Golebiowski, C. R. Johnson, Tetrahedron 1996, 52, 3769-3826.
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For the resolution of allylic alcohols by asymmetric catalysis, see: a) V. S. Martin, S. S. Woodard, T. Katsuki, Y. Yamada, M. Ikeda, K. B. Sharpless, J. Am. Chem. Soc. 1981, 103, 6237-6240; b) Y. Kitano, T. Matsumoto, F. Sato, J. Chem. Soc. Chem. Commun. 1986, 1323-1325; c) M. Kitamura, K. Manabe, R. Noyori, H. Takaya, Tetrahedron Lett. 1987, 28, 4719-4720; d) M. Kitamura, I. Kasahara, K. Manabe, R. Noyori, H. Takaya, J. Org. Chem. 1988, 53, 708-710.
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For the resolution of allylic alcohols by asymmetric catalysis, see: a) V. S. Martin, S. S. Woodard, T. Katsuki, Y. Yamada, M. Ikeda, K. B. Sharpless, J. Am. Chem. Soc. 1981, 103, 6237-6240; b) Y. Kitano, T. Matsumoto, F. Sato, J. Chem. Soc. Chem. Commun. 1986, 1323-1325; c) M. Kitamura, K. Manabe, R. Noyori, H. Takaya, Tetrahedron Lett. 1987, 28, 4719-4720; d) M. Kitamura, I. Kasahara, K. Manabe, R. Noyori, H. Takaya, J. Org. Chem. 1988, 53, 708-710.
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33845278869
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For the resolution of allylic alcohols by asymmetric catalysis, see: a) V. S. Martin, S. S. Woodard, T. Katsuki, Y. Yamada, M. Ikeda, K. B. Sharpless, J. Am. Chem. Soc. 1981, 103, 6237-6240; b) Y. Kitano, T. Matsumoto, F. Sato, J. Chem. Soc. Chem. Commun. 1986, 1323-1325; c) M. Kitamura, K. Manabe, R. Noyori, H. Takaya, Tetrahedron Lett. 1987, 28, 4719-4720; d) M. Kitamura, I. Kasahara, K. Manabe, R. Noyori, H. Takaya, J. Org. Chem. 1988, 53, 708-710.
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Reviews on chemical kinetic resolution: H. B. Kagan, J. C. Fiaud, Top. Stereochem. 1988, 18, 249-330; J. M. Brown, Chem. Ber. 1989, 25, 276-280; R. Noyori, M. Tokunaga, M. Kitamura, Biol. Chem. Soc. Jpn. 1995, 68, 36-55.
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Reviews on chemical kinetic resolution: H. B. Kagan, J. C. Fiaud, Top. Stereochem. 1988, 18, 249-330; J. M. Brown, Chem. Ber. 1989, 25, 276-280; R. Noyori, M. Tokunaga, M. Kitamura, Biol. Chem. Soc. Jpn. 1995, 68, 36-55.
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Reviews on chemical kinetic resolution: H. B. Kagan, J. C. Fiaud, Top. Stereochem. 1988, 18, 249-330; J. M. Brown, Chem. Ber. 1989, 25, 276-280; R. Noyori, M. Tokunaga, M. Kitamura, Biol. Chem. Soc. Jpn. 1995, 68, 36-55.
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For examples of catalytic asymmetric reduction of simple alkyl aryl ketones, see: a) T. Ohkuma, H. Ooka, S. Hashiguchi, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 2675-2676; b) E. J. Corey, R. K. Bakshi, S. Shibata, ibid. 1987, 109, 5551-5553; c) H. Nishiyama, H. Sakaguchi, T. Nakamura, M. Horihata, M. Kondo, K. Itoh, Organometallics 1989, 8, 846-848.
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For examples of catalytic asymmetric reduction of simple alkyl aryl ketones, see: a) T. Ohkuma, H. Ooka, S. Hashiguchi, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 2675-2676; b) E. J. Corey, R. K. Bakshi, S. Shibata, ibid. 1987, 109, 5551-5553; c) H. Nishiyama, H. Sakaguchi, T. Nakamura, M. Horihata, M. Kondo, K. Itoh, Organometallics 1989, 8, 846-848.
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For examples of catalytic asymmetric reduction of simple alkyl aryl ketones, see: a) T. Ohkuma, H. Ooka, S. Hashiguchi, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 2675-2676; b) E. J. Corey, R. K. Bakshi, S. Shibata, ibid. 1987, 109, 5551-5553; c) H. Nishiyama, H. Sakaguchi, T. Nakamura, M. Horihata, M. Kondo, K. Itoh, Organometallics 1989, 8, 846-848.
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For 6 with a high ee, see: [11d] (kinetic resolution). See also: a) M. Kawasaki, Y. Suzuki, S. Terashima, Chem. Lett. 1984, 239-242; b) T. Sato, Y. Goto, Y. Wakabayashi, T. Fujisawa, Tetrahedron Lett. 1983, 24, 4123-4126 (stoichiometric asymmetric reduction).
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stoichiometric asymmetric reduction
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For 6 with a high ee, see: [11d] (kinetic resolution). See also: a) M. Kawasaki, Y. Suzuki, S. Terashima, Chem. Lett. 1984, 239-242; b) T. Sato, Y. Goto, Y. Wakabayashi, T. Fujisawa, Tetrahedron Lett. 1983, 24, 4123-4126 (stoichiometric asymmetric reduction).
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