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Volumn 13, Issue 23, 2002, Pages 2605-2608

New chiral N-(N,N-dialkylamino)sulfamoyl-1,2-diamine ligands for highly enantioselective transfer hydrogenation of ketones

Author keywords

[No Author keywords available]

Indexed keywords

DIAMINE DERIVATIVE; KETONE DERIVATIVE; LIGAND; RHENIUM COMPLEX; RUTHENIUM COMPLEX;

EID: 0037180582     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(02)00659-6     Document Type: Article
Times cited : (68)

References (20)
  • 2
    • 0003544583 scopus 로고
    • Ojima, I., Ed.; VCH: New York; Chapter 6
    • Hydrosilylation: (a) Brunner, H.; Nishiyama, H.; Itoh, K. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993; Chapter 6; (b) Sun, J.; Buchwald, S. L. J. Am. Chem. Soc. 1999, 121, 5640; (c) Haslam, E. Shikimic Acid Metabolism and Metabolites; John Wiley & Sons: New York, 1993.
    • (1993) Catalytic Asymmetric Synthesis
    • Brunner, H.1    Nishiyama, H.2    Itoh, K.3
  • 3
    • 0033597622 scopus 로고    scopus 로고
    • Hydrosilylation: (a) Brunner, H.; Nishiyama, H.; Itoh, K. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993; Chapter 6; (b) Sun, J.; Buchwald, S. L. J. Am. Chem. Soc. 1999, 121, 5640; (c) Haslam, E. Shikimic Acid Metabolism and Metabolites; John Wiley & Sons: New York, 1993.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 5640
    • Sun, J.1    Buchwald, S.L.2
  • 4
    • 0004112742 scopus 로고
    • John Wiley & Sons: New York
    • Hydrosilylation: (a) Brunner, H.; Nishiyama, H.; Itoh, K. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993; Chapter 6; (b) Sun, J.; Buchwald, S. L. J. Am. Chem. Soc. 1999, 121, 5640; (c) Haslam, E. Shikimic Acid Metabolism and Metabolites; John Wiley & Sons: New York, 1993.
    • (1993) Shikimic Acid Metabolism and Metabolites
    • Haslam, E.1
  • 5
    • 0003013946 scopus 로고
    • Hydroboration: (a) Singh, V. K. Synthesis 1991, 605; (b) Brown, J. M.; Hulmes, D. I.; Layzell, T. P. J. Chem. Soc., Chem. Commun. 1993, 1673.
    • (1991) Synthesis , pp. 605
    • Singh, V.K.1
  • 7
    • 4243378570 scopus 로고
    • For reviews, see: (a) Zassinovich, G.; Mestroni, G.; Gladiali, S. Chem. Rev. 1992, 92, 1051; (b) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97; (c) Palmer, M. J.; Wills, M. Tetrahedron: Asymmetry 1999, 10, 2045.
    • (1992) Chem. Rev. , vol.92 , pp. 1051
    • Zassinovich, G.1    Mestroni, G.2    Gladiali, S.3
  • 8
    • 0002123299 scopus 로고    scopus 로고
    • For reviews, see: (a) Zassinovich, G.; Mestroni, G.; Gladiali, S. Chem. Rev. 1992, 92, 1051; (b) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97; (c) Palmer, M. J.; Wills, M. Tetrahedron: Asymmetry 1999, 10, 2045.
    • (1997) Acc. Chem. Res. , vol.30 , pp. 97
    • Noyori, R.1    Hashiguchi, S.2
  • 9
    • 0033522739 scopus 로고    scopus 로고
    • For reviews, see: (a) Zassinovich, G.; Mestroni, G.; Gladiali, S. Chem. Rev. 1992, 92, 1051; (b) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97; (c) Palmer, M. J.; Wills, M. Tetrahedron: Asymmetry 1999, 10, 2045.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 2045
    • Palmer, M.J.1    Wills, M.2
  • 16
    • 0011964227 scopus 로고    scopus 로고
    • note
    • 2-DPEN ligands and their results will be communicated in due course.
  • 17
    • 0011938775 scopus 로고    scopus 로고
    • note
    • 13 94% ee, >99% conversion; -with 2-carbomethoxy-1-indanone: >99% ee, >99% de, 48% conversion after 48 h (this work).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.