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Volumn 37, Issue 13-14, 1998, Pages 1827-1830

Highly enantioselective complex-catalyzed reduction of ketones - Now with purely aliphatic derivatives too

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EID: 0032479763     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19980803)37:13/14<1827::AID-ANIE1827>3.0.CO;2-C     Document Type: Article
Times cited : (50)

References (52)
  • 2
    • 0032482106 scopus 로고    scopus 로고
    • Q. Jiang, Y. Jiang, D. Xiao, P. Cao, X. Zhang, Angew. Chem. 1998, 110, 1203-1207; Angew. Chem. Int. Ed. 1998, 37, 1100-1103.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1100-1103
  • 3
    • 0026085360 scopus 로고
    • In the case of purely aliphatic ketones such as nonan-3-one, use of an alcohol dehydrogenase extracted from Gluconobacter oxidans (ATCC 621) results in enantioselectivities of up to 95%: P. Adlercreuz, Enzyme Mikrob. Technol. 1991, 13, 9-14.
    • (1991) Enzyme Mikrob. Technol. , vol.13 , pp. 9-14
    • Adlercreuz, P.1
  • 15
    • 0003400107 scopus 로고
    • Wiley, New York
    • for a review of subsequent work, see c) R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994, 61-82; d) T. Ohkuma, H. Ooka, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 10417-10418; e) T. Ohkuma, H. Ikehira, T. Ikariya, R. Noyori, Synlett 1997, 467-468; f) J.-P. Tranchier, V. Ratovelomanana-Vidal, J.-P. Genet, S. Tony, T. Cohen, Tetrahedron Lett. 1997, 38, 2951-2954; g) T. Ohta, T. Miyake, N. Seido, H. Kumobayashi, H. Takaya, J. Org. Chem. 1995, 60, 357-363; h) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1087.
    • (1994) Asymmetric Catalysis in Organic Synthesis , pp. 61-82
    • Noyori, R.1
  • 16
    • 0000239724 scopus 로고
    • for a review of subsequent work, see c) R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994, 61-82; d) T. Ohkuma, H. Ooka, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 10417-10418; e) T. Ohkuma, H. Ikehira, T. Ikariya, R. Noyori, Synlett 1997, 467-468; f) J.-P. Tranchier, V. Ratovelomanana-Vidal, J.-P. Genet, S. Tony, T. Cohen, Tetrahedron Lett. 1997, 38, 2951-2954; g) T. Ohta, T. Miyake, N. Seido, H. Kumobayashi, H. Takaya, J. Org. Chem. 1995, 60, 357-363; h) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1087.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10417-10418
    • Ohkuma, T.1    Ooka, H.2    Ikariya, T.3    Noyori, R.4
  • 17
    • 0000143557 scopus 로고    scopus 로고
    • for a review of subsequent work, see c) R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994, 61-82; d) T. Ohkuma, H. Ooka, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 10417-10418; e) T. Ohkuma, H. Ikehira, T. Ikariya, R. Noyori, Synlett 1997, 467-468; f) J.-P. Tranchier, V. Ratovelomanana-Vidal, J.-P. Genet, S. Tony, T. Cohen, Tetrahedron Lett. 1997, 38, 2951-2954; g) T. Ohta, T. Miyake, N. Seido, H. Kumobayashi, H. Takaya, J. Org. Chem. 1995, 60, 357-363; h) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1087.
    • (1997) Synlett , pp. 467-468
    • Ohkuma, T.1    Ikehira, H.2    Ikariya, T.3    Noyori, R.4
  • 18
    • 0030935322 scopus 로고    scopus 로고
    • for a review of subsequent work, see c) R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994, 61-82; d) T. Ohkuma, H. Ooka, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 10417-10418; e) T. Ohkuma, H. Ikehira, T. Ikariya, R. Noyori, Synlett 1997, 467-468; f) J.-P. Tranchier, V. Ratovelomanana-Vidal, J.-P. Genet, S. Tony, T. Cohen, Tetrahedron Lett. 1997, 38, 2951-2954; g) T. Ohta, T. Miyake, N. Seido, H. Kumobayashi, H. Takaya, J. Org. Chem. 1995, 60, 357-363; h) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1087.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 2951-2954
    • Tranchier, J.-P.1    Ratovelomanana-Vidal, V.2    Genet, J.-P.3    Tony, S.4    Cohen, T.5
  • 19
    • 33751155033 scopus 로고
    • for a review of subsequent work, see c) R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994, 61-82; d) T. Ohkuma, H. Ooka, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 10417-10418; e) T. Ohkuma, H. Ikehira, T. Ikariya, R. Noyori, Synlett 1997, 467-468; f) J.-P. Tranchier, V. Ratovelomanana-Vidal, J.-P. Genet, S. Tony, T. Cohen, Tetrahedron Lett. 1997, 38, 2951-2954; g) T. Ohta, T. Miyake, N. Seido, H. Kumobayashi, H. Takaya, J. Org. Chem. 1995, 60, 357-363; h) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1087.
    • (1995) J. Org. Chem. , vol.60 , pp. 357-363
    • Ohta, T.1    Miyake, T.2    Seido, N.3    Kumobayashi, H.4    Takaya, H.5
  • 20
    • 0032506982 scopus 로고    scopus 로고
    • for a review of subsequent work, see c) R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994, 61-82; d) T. Ohkuma, H. Ooka, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 10417-10418; e) T. Ohkuma, H. Ikehira, T. Ikariya, R. Noyori, Synlett 1997, 467-468; f) J.-P. Tranchier, V. Ratovelomanana-Vidal, J.-P. Genet, S. Tony, T. Cohen, Tetrahedron Lett. 1997, 38, 2951-2954; g) T. Ohta, T. Miyake, N. Seido, H. Kumobayashi, H. Takaya, J. Org. Chem. 1995, 60, 357-363; h) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1087.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1086-1087
    • Ohkuma, T.1    Doucet, H.2    Pham, T.3    Mikami, K.4    Korenaga, T.5    Terada, M.6    Noyori, R.7
  • 26
    • 0032479254 scopus 로고    scopus 로고
    • b) H. Doucet, T. Ohkuma, K. Murata, T. Yokozawa, M. Kozawa, E. Katayama, A. F. England, T. Ikariya, R. Noyori, Angew. Chem. 1998, 110, 1792-1776, Angew. Chem. Int. Ed. 1998, 37, 1703-1707.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1703-1707
  • 28
    • 0006337248 scopus 로고
    • T. Nagata, K. Yorozu, T. Yamada, T. Mukaiyama, Angew. Chem. 1995, 107, 2309-2311; Angew. Chem. Int. Ed. Engl. 1995, 34, 2145-2147. For a recent review on the asymmetric reduction of carbonyl groups with hydrides, see J. Seyden-Penne, Reductions by the Alumino-and Borohydrides in Organic Synthesis, 2nd ed., Wiley, New York, 1997, 55-84.
    • (1995) Angew. Chem. , vol.107 , pp. 2309-2311
    • Nagata, T.1    Yorozu, K.2    Yamada, T.3    Mukaiyama, T.4
  • 29
    • 33748216114 scopus 로고
    • T. Nagata, K. Yorozu, T. Yamada, T. Mukaiyama, Angew. Chem. 1995, 107, 2309-2311; Angew. Chem. Int. Ed. Engl. 1995, 34, 2145-2147. For a recent review on the asymmetric reduction of carbonyl groups with hydrides, see J. Seyden-Penne, Reductions by the Alumino-and Borohydrides in Organic Synthesis, 2nd ed., Wiley, New York, 1997, 55-84.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 2145-2147
  • 30
    • 0003932751 scopus 로고    scopus 로고
    • Wiley, New York
    • T. Nagata, K. Yorozu, T. Yamada, T. Mukaiyama, Angew. Chem. 1995, 107, 2309-2311; Angew. Chem. Int. Ed. Engl. 1995, 34, 2145-2147. For a recent review on the asymmetric reduction of carbonyl groups with hydrides, see J. Seyden-Penne, Reductions by the Alumino-and Borohydrides in Organic Synthesis, 2nd ed., Wiley, New York, 1997, 55-84.
    • (1997) Reductions by the Alumino- and Borohydrides in Organic Synthesis, 2nd Ed. , pp. 55-84
    • Seyden-Penne, J.1
  • 31
    • 0002123299 scopus 로고    scopus 로고
    • Review: a) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-112; b) K. Matsumura, S. Hashiguchi, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1997, 119, 8738-8739.
    • (1997) Acc. Chem. Res. , vol.30 , pp. 97-112
    • Noyori, R.1    Hashiguchi, S.2
  • 46
    • 0000060624 scopus 로고    scopus 로고
    • b) J. Albrecht, U. Nagel, Angew. Chem. 1996, 108, 444-446; Angew. Chem. Int. Ed. Engl. 1996, 55, 404-407.
    • (1996) Angew. Chem. , vol.108 , pp. 444-446
    • Albrecht, J.1    Nagel, U.2
  • 47
    • 84889444506 scopus 로고    scopus 로고
    • b) J. Albrecht, U. Nagel, Angew. Chem. 1996, 108, 444-446; Angew. Chem. Int. Ed. Engl. 1996, 55, 404-407.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.55 , pp. 404-407
  • 50
    • 25544461141 scopus 로고    scopus 로고
    • (BASF AG), personal communication
    • R. Stürmer (BASF AG), personal communication.
    • Stürmer, R.1
  • 51
    • 0000124466 scopus 로고    scopus 로고
    • Review: K. Mori, Chem. Commun. 1997, 13, 1153-1158.
    • (1997) Chem. Commun. , vol.13 , pp. 1153-1158
    • Mori, K.1


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