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Volumn 58, Issue 44, 2002, Pages 8993-8999

Synthesis and selective anion recognition of imidazolium cyclophanes

Author keywords

Cyclophane; Hydrogen bond; Imidazole derivative; Molecular recognition; X ray crystal structure

Indexed keywords

ACETONITRILE; ANION; BENZENE; BENZIMIDAZOLIUM; BROMINE DERIVATIVE; CYCLOPHANE; DIBROMIDE; DIMETHYL SULFOXIDE; FUNCTIONAL GROUP; HALIDE; HYDROGEN; IMIDAZOLE DERIVATIVE; IMIDAZOLIUM CYCLOPHANE; MACROCYCLIC COMPOUND; PROTON; UNCLASSIFIED DRUG; XYLENE;

EID: 0037191028     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)01153-5     Document Type: Article
Times cited : (87)

References (15)
  • 1
  • 2
    • 0035793285 scopus 로고    scopus 로고
    • A. Bianchi, K. Bowman-James, & E. García-España. Wiley-VCH New York (e)
    • Beer P.D., Gale P.A. Angew. Chem., Int. Ed. 40:2001;486 (b) Beer P.D. Acc. Chem. Res. 31:1998;71 (c) Schmidtchen F.P., Berger M. Chem. Rev. 97:1997;1609 (d) Bianchi A., Bowman-James K., García-España E., Supramolecular Chemistry of Anions. 1997;Wiley-VCH, New York, (e) Gale P.A. Coord. Chem. Rev. 199:2000;181 (f) Antonisse M.M.G., Reinhoudt D.N. Chem. Commun. 1998;443 (g) Gale P.A., Sessler J.L., Král V. Chem. Commun. 1998;1.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 486
    • Beer, P.D.1    Gale, P.A.2
  • 3
    • 0011167780 scopus 로고    scopus 로고
    • J.-M. Lehn, J.L. Atwood, J.E.D. Davies, D.D. MacNicol, & F. Vögtle. Elsevier Oxford (b)
    • Seel C., de Mendoza J. Lehn J.-M., Atwood J.L., Davies J.E.D., MacNicol D.D., Vögtle F., Comprehensive Supramolecular Chemistry. Vol. 2:1996;Elsevier, Oxford, (b) Vögtle F. Cyclophane Chemistry. 1993;Wiley, Chichester, (c) Seel C., Vögtle F. Angew. Chem., Int. Ed. Engl. 31:1992;528 (d) Diederich F. Stoddart J.F., Cyclophanes, Monographs in Supramolecular Chemistry. 1991;Royal Society of Chemistry, Cambridge.
    • (1996) Comprehensive Supramolecular Chemistry , vol.2 , pp. 528
    • Seel, C.1    De Mendoza, J.2
  • 4
    • 0011213896 scopus 로고    scopus 로고
    • note
    • Examples of cyclophanes as hosts for anion recognition: (a)
  • 5
    • 0035150259 scopus 로고    scopus 로고
    • . Examples of cyclophanes as hosts for anion recognition: (a) Szumna A., Jurczak J. Eur. J. Org. Chem. 2001;4031 (b) Sasaki S., Mizuno M., Naemura K., Tobe Y.J. J. Org. Chem. 65:2000;275 (c) Reuter C., Wienard W., Hübner G.N., Seel C., Vögtle F. Angew. Chem., Int. Ed. Engl. 38:1999;383 (d) Tanaka A., Fujiyoshi S., Motomura K., Hayashida O., Hiseada Y., Murakami Y. Tetrahedron. 54:1998;5187 (e) Beer P.D., Szemes F., Balzani V., Salà C.M., Drew N.G.B., Dent S.W., Maestri M. J. Am. Chem. Soc. 119:1997;11864 (f) Bisson A.P., Lynch V.M., Monahan M.-K.C., Anslyn E.V. J. Am. Chem. Soc. 119:1997;2340 (g) Hinzeu B., Seiler P., Diederich F. Helv. Chim. Acta. 79:1996;942.
    • (2001) Eur. J. Org. Chem. , vol.65 , pp. 4031
    • Szumna, A.1    Jurczak, J.2
  • 6
    • 0003719912 scopus 로고    scopus 로고
    • Springer New York (b)
    • Dugas H. Bioorganic Chemistry. 3rd ed. 1996;Springer, New York, (b) Hamilton A.D. Dugas H., Bioorganic Chemistry Frontiers. Vol. 2:1992;Springer, New York.
    • (1996) Bioorganic Chemistry 3rd ed. , vol.2
    • Dugas, H.1
  • 7
    • 0037117786 scopus 로고    scopus 로고
    • Wisner J.A., Beer P.D., Berry N.G., Tomapatanaget B. Proc. Natl Acad. Sci. USA. 99:2002;4983 (b) Howarth J. Recent Res. Dev. Org. Chem. 4:2000;155 (c) Aakeroy C.B., Evans T.A., Seddon K.R., Palinko I. New J. Chem. 1999;145 (d) Elaiwi A., Hitchcock P.B., Seddon K.R., Srinivasan N., Tan Y.-M., Welton T., Zora J.A. J. Chem. Soc., Dalton Trans. 1995;3467 (e) Avent A.G., Chaloner P.A., Day M.P., Seddon K.R., Welton T. J. Chem. Soc., Dalton Trans. 1994;3405.
    • (2002) Proc. Natl Acad. Sci. USA , vol.99 , pp. 4983
    • Wisner, J.A.1    Beer, P.D.2    Berry, N.G.3    Tomapatanaget, B.4
  • 12
    • 0033582512 scopus 로고    scopus 로고
    • Cabildo P., Sanz D., Claramunt R.M., Bourne S.A., Alkorta I., Elguero J. Tetrahedron. 55:1999;2327 (b) Alcalde E., Ramos S., Pérez-García L. Org. Lett. 1:1999;1035 (c) Alcalde E., Alemany M., Gisbert M. Tetrahedron. 52:1996;15171 (d) Alcalde E., Gisbert M. Synlett. 1996;285 (e) Alcalde E., Alemany M., Pérez-García L., Rodriguez M.L. J. Chem. Soc., Chem. Commun. 1995;1239.
    • (1999) Tetrahedron , vol.55 , pp. 2327
    • Cabildo, P.1    Sanz, D.2    Claramunt, R.M.3    Bourne, S.A.4    Alkorta, I.5    Elguero, J.6
  • 13
    • 0029855827 scopus 로고    scopus 로고
    • Examples of the UV-visible titrimetric method being used in molecular recognition: (a)
  • 14
    • 0035804947 scopus 로고    scopus 로고
    • VCH Weinheim (b)
    • Examples of the UV-visible titrimetric method being used in molecular recognition: (a) Chen G., John T., Alcala M., Mallouk T.E. J. Org. Chem. 66:2001;3027 (b) Kimura E., Kitamura H., Ohtani K., Koike T. J. Am. Chem. Soc. 122:2000;4668 (c) Black C.B., Andrioletti B., Try A.C., Ruiperez C., Sessler J.L. J. Am. Chem. Soc. 121:1999;10438 (d) Watanabe S., Onogawa O., Komatsu Y., Yoshida K. J. Am. Chem. Soc. 120:1998;229 (e) Liu Y., Li B., Han B.-H., Li Y.-M., Chen R.-T. J. Chem. Soc., Perkin Trans. 2. 1997;1275 (f) Asakawa M., Brown C.L., Pasini D., Stoddart J.F., Wyatt P.G. J. Org. Chem. 61:1996;7234 (g) Kuroda Y., Kato Y., Higashioji T., Hasegawa J.-, Kawanami S., Takahashi M., Shiraishi N., Tanabe K., Ogoshi H. J. Am. Chem. Soc. 117:1995;10950 (h) Mizutani T., Ema T., Tomita T., Kuroda Y., Ogoshi H. J. Am. Chem. Soc. 116:1994;4240.
    • (2001) J. Org. Chem. , vol.66 , pp. 3027
    • Chen, G.1    John, T.2    Alcala, M.3    Mallouk, T.E.4


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