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Volumn 16, Issue 14, 1997, Pages 3091-3093

Synthesis, structures, and reactivities of rhodium and ruthenium complexes with a novel chiral cyclopentadienyl-ferrocenyldiphenylphosphine bidentate ligand

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Indexed keywords


EID: 0000042251     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9702385     Document Type: Article
Times cited : (56)

References (47)
  • 1
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    • For reviews, see: (a) Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993. (b) Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley: New York, 1994. (c) Brunner, H.; Zettimeier, W. Handbook of Enantioselective Catalysis with Transition Metal Compounds; VCH: Weinheim, Germany, 1993.
    • (1993) Catalytic Asymmetric Synthesis
    • Ojima, I.1
  • 2
    • 0003400107 scopus 로고
    • Wiley: New York
    • For reviews, see: (a) Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993. (b) Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley: New York, 1994. (c) Brunner, H.; Zettimeier, W. Handbook of Enantioselective Catalysis with Transition Metal Compounds; VCH: Weinheim, Germany, 1993.
    • (1994) Asymmetric Catalysis in Organic Synthesis
    • Noyori, R.1
  • 5
    • 1642548577 scopus 로고
    • and references cited therein
    • (b) Halterman, R. L. Chem. Rev. 1992, 92, 965 and references cited therein.
    • (1992) Chem. Rev. , vol.92 , pp. 965
    • Halterman, R.L.1
  • 11
    • 0000293467 scopus 로고    scopus 로고
    • and references cited therein
    • (a) Trost, B. M. Chem. Ber. 1996, 129, 1313 and references cited therein.
    • (1996) Chem. Ber. , vol.129 , pp. 1313
    • Trost, B.M.1
  • 15
    • 85033188623 scopus 로고    scopus 로고
    • Transition Metal Sulfur Chemistry; Stiefel, E. I., Matsumoto, K., Eds.; American Chemical Society: Washington, DC
    • (a) Hidai, M.; Mizobe, Y. In Transition Metal Sulfur Chemistry; Stiefel, E. I., Matsumoto, K., Eds.; ACS Synposium Series 653; American Chemical Society: Washington, DC, 1996.
    • (1996) ACS Synposium Series 653
    • Hidai, M.1    Mizobe, Y.2
  • 25
    • 0029782396 scopus 로고    scopus 로고
    • VCH: Weinheim, Germany
    • For reviews, see: (a) Ferrocenes; Togni, A., Hayashi, T., Eds.; VCH: Weinheim, Germany, 1995. (b) Togni, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 1475.
    • (1995) Ferrocenes
    • Togni, A.1    Hayashi, T.2
  • 26
    • 0029782396 scopus 로고    scopus 로고
    • For reviews, see: (a) Ferrocenes; Togni, A., Hayashi, T., Eds.; VCH: Weinheim, Germany, 1995. (b) Togni, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 1475.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 1475
    • Togni, A.1
  • 34
    • 85033170569 scopus 로고    scopus 로고
    • note
    • 26-FeOPRh: C, 60.84; H, 4.43. Found: C, 60.59; H, 4.08.
  • 35
    • 85033168074 scopus 로고    scopus 로고
    • note
    • w = 0.023 for 4109 unique reflections (I > 3σ(I)).
  • 36
    • 85033182901 scopus 로고    scopus 로고
    • note
    • 2Ru·2EtOH: C, 64.34; H, 5.61. Found: C, 64.10; H, 5.28.
  • 37
    • 85033189847 scopus 로고    scopus 로고
    • note
    • w = 0.084 for 3960 unique reflections (I > 3σ(I)).
  • 40
    • 85033175224 scopus 로고    scopus 로고
    • note
    • 3Ru: C, 61.58; H, 4.51. Found: C, 61.19; H, 4.89.
  • 41
    • 85033163318 scopus 로고    scopus 로고
    • note
    • -1, R = 0.078, Rw = 0.085 for 1944 unique reflections (I > 3σ(I)). The carbon atoms of cyclopentadienyl rings and ruthenium, iron, and phosphine atoms were refined anisotropically. All other non-hydrogen atoms were refined isotropically.
  • 46
    • 85033181820 scopus 로고    scopus 로고
    • note
    • The low yield of 7 for both the stoichiometric and catalytic reactions was due to the formation of unidentified side products.
  • 47
    • 85033183458 scopus 로고    scopus 로고
    • note
    • The preliminary results of a few catalytic reactions using 5 are as follows: 1-octyne and 1-buten-3-ol (20%, 34% ee), 1-octyne and 4-methyl-1-penten-3-ol (10%, 27% ee). The results will be reported in due course.


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