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Volumn 9, Issue 2, 1997, Pages 96-98

Is chiral recognition a three-point process?

Author keywords

chiral separations; enantioselectivity; stereospecificity

Indexed keywords

BIOPOLYMER;

EID: 0030936156     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(1997)9:2<96::AID-CHIR2>3.0.CO;2-E     Document Type: Conference Paper
Times cited : (97)

References (11)
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    • Burger, A., ed. New York: Wiley-Interscience
    • Burger, A. Relation of chemical structure and biological activity. In: Medicinal Chemistry, 3rd ed. Burger, A., ed. New York: Wiley-Interscience, 1970:64-80.
    • (1970) Medicinal Chemistry, 3rd Ed. , pp. 64-80
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    • The optical resolution of aromatic amino acids on paper chromatograms
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    • Pirkle, W.H., Pochapsky, T.C., Burke, J.A. III, Deming, K.C. Systematic studies of chiral recognition mechanisms. In: Chiral Separations. Stevenson, D., Wilson, I.D., eds. London: Plenum Press, 1988:23-36.
    • (1988) Chiral Separations , pp. 23-36
    • Pirkle, W.H.1    Pochapsky, T.C.2    Burke III, J.A.3    Deming, K.C.4
  • 8
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    • Einfluss der configuration auf die wirkung der enzyme
    • Fisher, E. Einfluss der configuration auf die wirkung der enzyme. Berl. Dtsch. Chem. Ges. 27:2985-2993, 1894.
    • (1894) Berl. Dtsch. Chem. Ges. , vol.27 , pp. 2985-2993
    • Fisher, E.1
  • 9
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    • Molecular structure and biological specificity
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    • (1948) Chem. Ind. (Suppl.) , pp. 1
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  • 10
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    • Enantioselectivity in two-point binding: Rocking tetrahedron model
    • Sokolov, V.I., Zefirov, N.S. Enantioselectivity in two-point binding: rocking tetrahedron model. Dokl. Akad. Nauk 319:1382-1383, 1991.
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  • 11
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    • Investigation of the enantioselecive separations of α-alkyl arylcarboxylic acids on an amylose tris (3,5-dimethylphenylcarbamate) chiral stationary phase using quantitative structure-enantioselective retention relationships (QSERR): Identification of a conformationally driven chiral rerognition mechanism
    • Booth, T.D., Wainer, I.W. Investigation of the enantioselecive separations of α-alkyl arylcarboxylic acids on an amylose tris (3,5-dimethylphenylcarbamate) chiral stationary phase using quantitative structure-enantioselective retention relationships (QSERR): identification of a conformationally driven chiral rerognition mechanism. J. Chromatogr. A 737:157-169, 1996.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.