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Volumn 39, Issue 2, 2006, Pages 31-39

Chiral, poly(rare-earth metal) complexes in asymmetric catalysis

Author keywords

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Indexed keywords


EID: 33646069329     PISSN: 00025100     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (55)

References (131)
  • 1
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    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: New York
    • (a) Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: New York, 2004.
    • (2004) Comprehensive Asymmetric Catalysis
  • 4
    • 33646057167 scopus 로고    scopus 로고
    • Beller, M., Bolm, C., Eds.; Wiley-VCH: Weinheim, Germany, Chapter 2.18
    • (a) Kobayashi, S. In Transition Metals for Organic Synthesis; Beller, M., Bolm, C., Eds.; Wiley-VCH: Weinheim, Germany, 1998; Vol. 1, Chapter 2.18.
    • (1998) Transition Metals for Organic Synthesis , vol.1
    • Kobayashi, S.1
  • 5
    • 0003441992 scopus 로고    scopus 로고
    • Yamamoto, H., Ed.; Wiley-VCH: Weinheim, Germany
    • (b) Lewis Acids in Organic Synthesis; Yamamoto, H., Ed.; Wiley-VCH: Weinheim, Germany, 2000.
    • (2000) Lewis Acids in Organic Synthesis
  • 6
    • 0001045470 scopus 로고
    • For selected examples of chiral, rare-earth-metal Lewis acid catalysts, see: (a) Kobayashi, S.; Ishitani, H. J. Am. Chem. Soc. 1994, 116, 4083.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 4083
    • Kobayashi, S.1    Ishitani, H.2
  • 14
  • 37
  • 50
    • 16844374787 scopus 로고    scopus 로고
    • For a review of combined acid catalysis, including Lewis acid assisted Lewis acid catalysis, see Yamamoto, H.; Futatsugi, K. Angew. Chem., Int. Ed. 2005, 44, 1924.
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 1924
    • Yamamoto, H.1    Futatsugi, K.2
  • 60
    • 0034698317 scopus 로고    scopus 로고
    • Recent reviews on: (a) The asymmetric epoxidation of electron-deficient C-C double bonds: Porter, M. J.; Skidmore, J. Chem. Commun. 2000, 1215.
    • (2000) Chem. Commun. , pp. 1215
    • Porter, M.J.1    Skidmore, J.2
  • 62
  • 76
    • 0034612973 scopus 로고    scopus 로고
    • Reviews of enantioselective conjugate additions: (a) Sibi, M. P.; Manyem, S. Tetrahedron 2000, 56, 8033.
    • (2000) Tetrahedron , vol.56 , pp. 8033
    • Sibi, M.P.1    Manyem, S.2
  • 83
  • 91
  • 99
    • 0032554099 scopus 로고    scopus 로고
    • For recent examples of advances in this field, see: (a) Dosa, P. I.; Fu, G. C. J. Am. Chem. Soc. 1998, 120, 445.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 445
    • Dosa, P.I.1    Fu, G.C.2
  • 121
    • 0034704642 scopus 로고    scopus 로고
    • For examples of the catalytic enantioselective Strecker reaction of keto imines reported by other groups, see: (a) Vachal, P.; Jacobsen, E. N. Org. Lett. 2000, 2, 867.
    • (2000) Org. Lett. , vol.2 , pp. 867
    • Vachal, P.1    Jacobsen, E.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.