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Volumn 60, Issue 36, 2004, Pages 7827-7833

Synthesis of an inherently chiral O,O′-bridged thiacalix[4] crowncarboxylic acid and its application to a chiral solvating agent

Author keywords

Calixarene; Calixcrown; Chiral recognition; Inherently chiral

Indexed keywords

AMINE; BROMOACETIC ACID; CARBOXYLIC ACID DERIVATIVE; CROWN ETHER DERIVATIVE; ESTER DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; TOLUENESULFONIC ACID DERIVATIVE;

EID: 4043095602     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.06.074     Document Type: Article
Times cited : (57)

References (65)
  • 1
    • 0003894828 scopus 로고    scopus 로고
    • For general overview of the calixarene chemistry, see: (a). Stoddart J.F. Cambridge: The Royal Society
    • For general overview of the calixarene chemistry, see: (a) Gutsche C.D. Stoddart J.F. Calixarenes Revisited, Monographs in Supramolecular Chemistry. Vol. 6:1998;The Royal Society, Cambridge
    • (1998) Calixarenes Revisited, Monographs in Supramolecular Chemistry , vol.6
    • Gutsche, C.D.1
  • 46
    • 0000019262 scopus 로고
    • Morrison J.D. New York: Academic
    • Weisman G.R. Morrison J.D. Asymmetric Synthesis. Vol. 1:1983;153-171 Academic, New York
    • (1983) Asymmetric Synthesis , vol.1 , pp. 153-171
    • Weisman, G.R.1
  • 57
    • 4043063093 scopus 로고    scopus 로고
    • 19 Thus, in acid (+)-6, the three phenolic oxygen atoms are fixed on the same side of the mean plane defined by the calixarene, one of which is chosen as a 'pilot atom'. According to the sequence rule, this is the oxygen which resides opposite to the hydroxy group. The sequence-rule-preferred path within the mean plane from the aromatic carbon attached to this oxygen toward that attached to the carboxymethoxy group traces counterclockwise tracks, which is denoted as S
  • 60
    • 33748216782 scopus 로고
    • 1H NMR spectra of rotaxane-like compounds consisting of a crown ether and a dialkylammonium ion, in which the β-proton signals of the ammonium ion shift to upfield as compared to those of the ammonium ion itself. See for example: (a)
    • 1H NMR spectra of rotaxane-like compounds consisting of a crown ether and a dialkylammonium ion, in which the β-proton signals of the ammonium ion shift to upfield as compared to those of the ammonium ion itself. See for example: (a) Ashton P.R., Campbell P.J., Chrystal E.J.T., Glink P.T., Menzer S., Philp D., Spencer N., Stoddart J.F., Tasker P.A., Williams D.J. Angew. Chem., Int. Ed. Engl. 34:1995;1865-1869
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1865-1869
    • Ashton, P.R.1    Campbell, P.J.2    Chrystal, E.J.T.3    Glink, P.T.4    Menzer, S.5    Philp, D.6    Spencer, N.7    Stoddart, J.F.8    Tasker, P.A.9    Williams, D.J.10
  • 63
    • 0003470466 scopus 로고    scopus 로고
    • Molecular Structure Corporation, 3200 Research Forest Drive, The Woodlands, TX 77381, USA; Rigaku, 3-9-12 Akishima, Tokyo, Japan.
    • TeXsan Single Crystal Structure Analysis Software, 1999. Molecular Structure Corporation, 3200 Research Forest Drive, The Woodlands, TX 77381, USA; Rigaku, 3-9-12 Akishima, Tokyo, Japan.
    • (1999) TeXsan Single Crystal Structure Analysis Software


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.