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Volumn 9, Issue 4, 1998, Pages 563-574

Preparation and temperature-dependent enantioselectivities of homochiral phenolic crown ethers having aryl chiral barriers: Thermodynamic parameters for enantioselective complexation with chiral amines

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; CHLOROFORM; CROWN ETHER DERIVATIVE; MANDELIC ACID; NAPHTHYL GROUP; PHENOL DERIVATIVE; TRIACYLGLYCEROL LIPASE;

EID: 0032570484     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00638-1     Document Type: Article
Times cited : (44)

References (18)
  • 1
    • 0004221649 scopus 로고
    • Springer-Verlag: New York
    • G. W. Gokel and S. H. Korezeniowski, Macrocyclic Polyether Syntheses; Springer-Verlag: New York, 1982; J. F. Stoddart, Chiral Crown Ethers. In Topics in Stereochemistry; E. L. Eliel and S. H. Wilen Eds.; Wiley-Interscience: New York, 1988; Vol. 17, p. 207; J.-M. Lehn, Supramolecular Chemistry; VCH Verlagsgesellachaft, Weinheim, 1955.
    • (1982) Macrocyclic Polyether Syntheses
    • Gokel, G.W.1    Korezeniowski, S.H.2
  • 2
    • 85023439502 scopus 로고
    • Chiral Crown Ethers
    • E. L. Eliel and S. H. Wilen Eds.; Wiley-Interscience: New York
    • G. W. Gokel and S. H. Korezeniowski, Macrocyclic Polyether Syntheses; Springer-Verlag: New York, 1982; J. F. Stoddart, Chiral Crown Ethers. In Topics in Stereochemistry; E. L. Eliel and S. H. Wilen Eds.; Wiley-Interscience: New York, 1988; Vol. 17, p. 207; J.-M. Lehn, Supramolecular Chemistry; VCH Verlagsgesellachaft, Weinheim, 1955.
    • (1988) In Topics in Stereochemistry; , vol.17 , pp. 207
    • Stoddart, J.F.1
  • 3
    • 0003699562 scopus 로고
    • VCH Verlagsgesellachaft, Weinheim
    • G. W. Gokel and S. H. Korezeniowski, Macrocyclic Polyether Syntheses; Springer-Verlag: New York, 1982; J. F. Stoddart, Chiral Crown Ethers. In Topics in Stereochemistry; E. L. Eliel and S. H. Wilen Eds.; Wiley-Interscience: New York, 1988; Vol. 17, p. 207; J.-M. Lehn, Supramolecular Chemistry; VCH Verlagsgesellachaft, Weinheim, 1955.
    • (1955) Supramolecular Chemistry
    • Lehn, J.-M.1
  • 11
    • 37049100138 scopus 로고
    • Y. Inoue and T. Hakushi, J. Chem. Soc., Perkin Trans. 2, 1985, 935; Y. Inoue, F. Amano, H. Inada, M. Ouchi, A. Tai, T. Hakushi, Y. Liu and L.-H. Tong, J. Chem. Soc., Perkin Trans. 2, 1990, 1239; Y. Inoue, T. Hakushi, Y. Liu, L.-H. Tong, B.-J. Shen and D.-S. Jin, J. Am. Chem. Soc., 1993, 115, 475.
    • (1985) J. Chem. Soc., Perkin Trans. 2 , pp. 935
    • Inoue, Y.1    Hakushi, T.2
  • 13
    • 0000223084 scopus 로고
    • Y. Inoue and T. Hakushi, J. Chem. Soc., Perkin Trans. 2, 1985, 935; Y. Inoue, F. Amano, H. Inada, M. Ouchi, A. Tai, T. Hakushi, Y. Liu and L.-H. Tong, J. Chem. Soc., Perkin Trans. 2, 1990, 1239; Y. Inoue, T. Hakushi, Y. Liu, L.-H. Tong, B.-J. Shen and D.-S. Jin, J. Am. Chem. Soc., 1993, 115, 475.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 475
    • Inoue, Y.1    Hakushi, T.2    Liu, Y.3    Tong, L.-H.4    Shen, B.-J.5    Jin, D.-S.6
  • 18
    • 0030575812 scopus 로고    scopus 로고
    • The authentic samples of both enantiomers of 8 were prepared according to the reported method;
    • The authentic samples of both enantiomers of 8 were prepared according to the reported method; K. Naemura, M. Murata, R. Tanaka, M. Yano, K. Hirose and Y. Tobe, Tetrahedron: Asymmetry, 1996, 7, 3285.
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 3285
    • Naemura, K.1    Murata, M.2    Tanaka, R.3    Yano, M.4    Hirose, K.5    Tobe, Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.