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Volumn 3, Issue 22, 2001, Pages 3435-3438

Asymmetric alkene epoxidation with chromium oxo salen complexes. A systematic study of salen ligand substituents

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ARTICLE;

EID: 0001644647     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol010144y     Document Type: Article
Times cited : (47)

References (27)
  • 3
    • 0000635013 scopus 로고    scopus 로고
    • Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: New York, Chapter 18.2
    • (b) Jacobsen, E. N.; Wu, M. H. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: New York, 1999; Chapter 18.2, pp 649-677.
    • (1999) Comprehensive Asymmetric Catalysis , pp. 649-677
    • Jacobsen, E.N.1    Wu, M.H.2
  • 4
    • 0002928569 scopus 로고    scopus 로고
    • Ojima, I., Ed.; Wiley-VCH: New York, Chapter 6B
    • (c) Katsuki, T. in Catalytic Asymmetric Synthesis, 2nd ed.; Ojima, I., Ed.; Wiley-VCH: New York, 2000; Chapter 6B, pp 287-325.
    • (2000) Catalytic Asymmetric Synthesis, 2nd Ed. , pp. 287-325
    • Katsuki, T.1
  • 9
    • 0041729880 scopus 로고    scopus 로고
    • note
    • For convenience, we refer to E-and Z-1,2-disubstituted alkenes as trans-and cis-alkenes, respectively.
  • 12
    • 0041729878 scopus 로고    scopus 로고
    • Abstracts of papers
    • New Orleans, LA.; American Chemical Society: Washington, DC, ORGN
    • Gilheany, D. G. Abstracts of Papers, 211th National Meeting of the American Chemical Society, New Orleans, LA.; American Chemical Society: Washington, DC, 1996; ORGN 165.
    • (1996) 211th National Meeting of the American Chemical Society , pp. 165
    • Gilheany, D.G.1
  • 13
    • 0043232494 scopus 로고    scopus 로고
    • note
    • 12 on these systems have revealed a great amount of detail about the exact nature of the distortions from planarity.
  • 15
    • 0030052488 scopus 로고    scopus 로고
    • Hamada, T.; Fukuda, T.; Imanishi, H.; Katsuki, T. Tetrahedron 1996, 52, 515-530; Hashihayata, T.; Ito, Y.; Katsuki, T. Synlett 1996, 1079; Hashihayata, T.; Ito, Y.; Katsuki, T. Tetrahedron 1997, 53, 9541-9552; Miura, K.; Katsuki, T. Synlett 1999, 783-785.
    • (1996) Tetrahedron , vol.52 , pp. 515-530
    • Hamada, T.1    Fukuda, T.2    Imanishi, H.3    Katsuki, T.4
  • 16
    • 0000899387 scopus 로고    scopus 로고
    • Hamada, T.; Fukuda, T.; Imanishi, H.; Katsuki, T. Tetrahedron 1996, 52, 515-530; Hashihayata, T.; Ito, Y.; Katsuki, T. Synlett 1996, 1079; Hashihayata, T.; Ito, Y.; Katsuki, T. Tetrahedron 1997, 53, 9541-9552; Miura, K.; Katsuki, T. Synlett 1999, 783-785.
    • (1996) Synlett , pp. 1079
    • Hashihayata, T.1    Ito, Y.2    Katsuki, T.3
  • 17
    • 0030874375 scopus 로고    scopus 로고
    • Hamada, T.; Fukuda, T.; Imanishi, H.; Katsuki, T. Tetrahedron 1996, 52, 515-530; Hashihayata, T.; Ito, Y.; Katsuki, T. Synlett 1996, 1079; Hashihayata, T.; Ito, Y.; Katsuki, T. Tetrahedron 1997, 53, 9541-9552; Miura, K.; Katsuki, T. Synlett 1999, 783-785.
    • (1997) Tetrahedron , vol.53 , pp. 9541-9552
    • Hashihayata, T.1    Ito, Y.2    Katsuki, T.3
  • 18
    • 0032997344 scopus 로고    scopus 로고
    • Hamada, T.; Fukuda, T.; Imanishi, H.; Katsuki, T. Tetrahedron 1996, 52, 515-530; Hashihayata, T.; Ito, Y.; Katsuki, T. Synlett 1996, 1079; Hashihayata, T.; Ito, Y.; Katsuki, T. Tetrahedron 1997, 53, 9541-9552; Miura, K.; Katsuki, T. Synlett 1999, 783-785.
    • (1999) Synlett , pp. 783-785
    • Miura, K.1    Katsuki, T.2
  • 22
    • 0032506979 scopus 로고    scopus 로고
    • and references therein
    • In addition to the known importance of the Z-position (ref 2), Jacobsen and co-workers have studied comprehensively substitution at the X position: Palucki, M.; Finney, N. S.; Pospisil, P. J.; Güler, M. L.; Ishida, T.; Jacobsen, E. N. J. Am. Chem. Soc. 1998, 120, 948-954 and references therein.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 948-954
    • Palucki, M.1    Finney, N.S.2    Pospisil, P.J.3    Güler, M.L.4    Ishida, T.5    Jacobsen, E.N.6
  • 23
    • 0043232495 scopus 로고    scopus 로고
    • note
    • 2O). analysis was by csp GLC on a Supelco α-cyclodextrin capillary column with n-decane as internal standard. Product configuration was determined and precursor chromiurn(III) - salen complexes prepared as described previously (ref 3d).
  • 26
    • 0346591845 scopus 로고
    • Hosoya, N.; Hatakeyama, A.; Yanai, K.; Fujii, H.; Irie, R.; Katsuki, T. Synlett 1993, 641-645. Hamada, T.; Irie, R.; Katsuki, T. Synlett 1994, 479-481.
    • (1994) Synlett , pp. 479-481
    • Hamada, T.1    Irie, R.2    Katsuki, T.3


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