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Volumn 125, Issue 29, 2003, Pages 8779-8789

Asymmetric hydrosilylation of aryl ketones catalyzed by copper hydride complexed by nonracemic biphenyl bis-phosphine ligands

Author keywords

[No Author keywords available]

Indexed keywords

HYDROSILYLATION;

EID: 0037960828     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja021391f     Document Type: Article
Times cited : (263)

References (73)
  • 1
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    • Asymmetric hydrosilylation and related reactions
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    • Nishiyarna, H.; Itoh, K. Asymmetric Hydrosilylation and Related Reactions. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; Wiley VCH: New York, 2000; Chapter 2.
    • (2000) Catalytic Asymmetric Synthesis
    • Nishiyarna, H.1    Itoh, K.2
  • 22
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    • Asymmetric hydrogenation
    • Ojima, I., Ed.; Wiley VCH: New York; Chapter 1 and references therein
    • Ohkuma, T.; Kitamura, M.; Noyori, R. Asymmetric Hydrogenation. In Catalytic Asymmetric Synthesis; Ojima. I., Ed.; Wiley VCH: New York, 2000; Chapter 1 and references therein.
    • (2000) Catalytic Asymmetric Synthesis
    • Ohkuma, T.1    Kitamura, M.2    Noyori, R.3
  • 29
    • 0038243069 scopus 로고    scopus 로고
    • note
    • Reagent of the Year, 1991; hydrido(triphenylphosphine)copper hexamer, CAS Registry No. 33636-93-0, Aldrich catalog #36,497-5.
  • 44
    • 0037905636 scopus 로고    scopus 로고
    • note
    • As a result of extensive and unexpected frothing, a considerable amount of the reaction mixture was lost, accounting for an isolated yield of only 48%. The TLC of the reaction mixture, as usual, was 'spot-to-spot'.
  • 57
    • 0037905635 scopus 로고    scopus 로고
    • note
    • Generously provided by Prof. A. Yudin, University of Toronto.
  • 64
    • 37049093369 scopus 로고
    • Such bonding schemes are well-established, however, for various complexes of Mn, Rh, and Mo. (a) Aspinall, H. C.; Deeming, A. J.; Donovan-Mtunzi, S. J. Chem. Soc. Dalton Trans. 1983, 2669. (b) Deraniyagala, S. P.; Grundy, K. R. Inorg. Chim. Acta 1984, 84, 205. (c) Curtis, M. D.; Klinger, R. J. J. Organomet. Chem. 1978, 161. 23. Curtis, M. D.; Han, K. R.; Butler, W. M. Inorg. Chem. 1980, 19, 2096.
    • (1983) J. Chem. Soc. Dalton Trans. , pp. 2669
    • Aspinall, H.C.1    Deeming, A.J.2    Donovan-Mtunzi, S.3
  • 65
    • 4243795812 scopus 로고
    • Such bonding schemes are well-established, however, for various complexes of Mn, Rh, and Mo. (a) Aspinall, H. C.; Deeming, A. J.; Donovan-Mtunzi, S. J. Chem. Soc. Dalton Trans. 1983, 2669. (b) Deraniyagala, S. P.; Grundy, K. R. Inorg. Chim. Acta 1984, 84, 205. (c) Curtis, M. D.; Klinger, R. J. J. Organomet. Chem. 1978, 161. 23. Curtis, M. D.; Han, K. R.; Butler, W. M. Inorg. Chem. 1980, 19, 2096.
    • (1984) Inorg. Chim. Acta , vol.84 , pp. 205
    • Deraniyagala, S.P.1    Grundy, K.R.2
  • 66
    • 0003091372 scopus 로고
    • Such bonding schemes are well-established, however, for various complexes of Mn, Rh, and Mo. (a) Aspinall, H. C.; Deeming, A. J.; Donovan-Mtunzi, S. J. Chem. Soc. Dalton Trans. 1983, 2669. (b) Deraniyagala, S. P.; Grundy, K. R. Inorg. Chim. Acta 1984, 84, 205. (c) Curtis, M. D.; Klinger, R. J. J. Organomet. Chem. 1978, 161. 23. Curtis, M. D.; Han, K. R.; Butler, W. M. Inorg. Chem. 1980, 19, 2096.
    • (1978) J. Organomet. Chem. , vol.161 , pp. 23
    • Curtis, M.D.1    Klinger, R.J.2
  • 67
    • 0040999683 scopus 로고
    • Such bonding schemes are well-established, however, for various complexes of Mn, Rh, and Mo. (a) Aspinall, H. C.; Deeming, A. J.; Donovan-Mtunzi, S. J. Chem. Soc. Dalton Trans. 1983, 2669. (b) Deraniyagala, S. P.; Grundy, K. R. Inorg. Chim. Acta 1984, 84, 205. (c) Curtis, M. D.; Klinger, R. J. J. Organomet. Chem. 1978, 161. 23. Curtis, M. D.; Han, K. R.; Butler, W. M. Inorg. Chem. 1980, 19, 2096.
    • (1980) Inorg. Chem. , vol.19 , pp. 2096
    • Curtis, M.D.1    Han, K.R.2    Butler, W.M.3
  • 68
    • 0037905634 scopus 로고    scopus 로고
    • note
    • 2 is evolved. Full details will be reported in due course.
  • 69
    • 0038243067 scopus 로고    scopus 로고
    • note
    • This trend argues against an 18 electron species (cf. Figure 3), as complexation of CuH by a π-bond of the biaryl ligand requires significant twisting, which increases the dihedral angle.
  • 71
    • 0001949253 scopus 로고
    • Fernelius, W. C., Ed.; McGraw-Hill: New York
    • Keller, R. N.; Wycoff. H. D. In Inorganic Syntheses Fernelius, W. C., Ed.; McGraw-Hill: New York, 1946; pp 1-4.
    • (1946) Inorganic Syntheses , pp. 1-4
    • Keller, R.N.1    Wycoff, H.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.