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Volumn 66, Issue 1, 2005, Pages 405-431

Remaekable effect of subtle structural change of chiral pseudo-18-crown-6 on enantiomer-selectivity in complexation with chiral amino alcohols

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EID: 33646858328     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-05-S(K)42     Document Type: Article
Times cited : (12)

References (45)
  • 2
    • 85023439502 scopus 로고
    • 'Chiral Crown Ethers'
    • Eliel E.L., and Wilen S.H. (Eds), Wiely-Interscience, New York
    • Stoddart J.F. 'Chiral Crown Ethers'. In: Eliel E.L., and Wilen S.H. (Eds). Topics in Stereochemistry Vol. 17 (1988), Wiely-Interscience, New York 207
    • (1988) Topics in Stereochemistry , vol.17 , pp. 207
    • Stoddart, J.F.1
  • 13
    • 84984249248 scopus 로고
    • For chirality indicators, see:
    • For chirality indicators, see:. Hollmann G., and Vögtle F. Chem. Ber. 117 (1984) 1355
    • (1984) Chem. Ber. , vol.117 , pp. 1355
    • Hollmann, G.1    Vögtle, F.2
  • 22
    • 0000078729 scopus 로고    scopus 로고
    • In the same year, Hyun and co-workers commercialized a chemically bonded type CSP named Chirosil RCA in which (+)-18-crown-6-2,3,11,12-tetracarboxylic acid was used as a selector
    • In the same year, Hyun and co-workers commercialized a chemically bonded type CSP named Chirosil RCA in which (+)-18-crown-6-2,3,11,12-tetracarboxylic acid was used as a selector. Hyun M.H., Jin J.S., and Lee W. Bull. Kor. Chem. Soc. 19 (1998) 819
    • (1998) Bull. Kor. Chem. Soc. , vol.19 , pp. 819
    • Hyun, M.H.1    Jin, J.S.2    Lee, W.3
  • 32
    • 33646865688 scopus 로고    scopus 로고
    • CCDC 282327 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif, or by emailing data_request@ccdc.cam.ac.uk, or by contacting The Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK.
  • 33
    • 37049133684 scopus 로고
    • 3 the signal of the methine proton appears at δ 4.00 as a doublet of doublet with J=10.9 and 4.7 Hz and that of trans-diastereomer appears at δ 3.78 as a broad triplet with J=2.5 Hz
    • 3 the signal of the methine proton appears at δ 4.00 as a doublet of doublet with J=10.9 and 4.7 Hz and that of trans-diastereomer appears at δ 3.78 as a broad triplet with J=2.5 Hz. Berti G., Macchia B., Macchia F., and Monti L. J. Chem. Soc. C 20 (1971) 3371
    • (1971) J. Chem. Soc. C , vol.20 , pp. 3371
    • Berti, G.1    Macchia, B.2    Macchia, F.3    Monti, L.4
  • 39
    • 33646863445 scopus 로고    scopus 로고
    • a=-(ΔH/R)(1/T)+(ΔS/R)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.