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Volumn 1, Issue 8, 1999, Pages 1217-1220

Sugar thioureas as anion receptors. Effect of intramolecular hydrogen bonding in the carboxylate binding properties of symmetric sugar thioureas

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EID: 0041622216     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol990889s     Document Type: Article
Times cited : (61)

References (36)
  • 6
    • 0005658210 scopus 로고    scopus 로고
    • Hudlicky, T., Ed.; JAI Press Ltd.: Greenwich, CT.
    • For leading references on artificial receptors for hydrogen-bond directed binding of carbohydrates, see: (a) Haseltine, J.; Doyle, T. J. Designed Hosts for Sugars. In Organic Synthesis. Theory and Applications; Hudlicky, T., Ed.; JAI Press Ltd.: Greenwich, CT. 1996; Vol. 3, p 85-107.
    • (1996) Organic Synthesis. Theory and Applications , vol.3 , pp. 85-107
    • Haseltine, J.1    Doyle, T.J.2
  • 25
    • 0028105027 scopus 로고
    • The stabilization of Z,E rotamers in sugar thioureas by seven-membered hydrogen bonds was supported by chemical shift temperature coefficient measurements, rotational barrier calculations and molecular modeling. It seems to be a main structural feature of this class of compounds, as seen from specifically designed models. See: (a) Ortiz Mellet, C.; Moreno Marín, A.; Jiménez Blanco, J. L.; García Fernández, J. M.; Fuentes, J. Tetrahedron: Asymmetry 1994, 5, 2325-2334.
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 2325-2334
    • Ortiz Mellet, C.1    Moreno Marín, A.2    Jiménez Blanco, J.L.3    García Fernández, J.M.4    Fuentes, J.5
  • 35
    • 0000381720 scopus 로고
    • The ability of chloroform to act as a hydrogen-bond donnor has been shwon, though it is a weak hydrogen-bond partner compared to amide-type protons. See: Sheridan, J. P.; Martire, D. E.; Tewari, Y. B. J. Am. Chem. Soc. 1972, 94, 3294-3248.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 3294-13248
    • Sheridan, J.P.1    Martire, D.E.2    Tewari, Y.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.