1. The Design of Drugs to Macromolecular Targets; Beddell, C.R., Ed. Wiley: Chichester, 1992.
2. Jinno, K.Chromatographic Separations Based on Molecular Recognition; Ed. VCH: Weinheim, 1996.
3. Marchi-Artzner, V.; Artzner, F.; Karthaus, O.; Shimomura, M.; Ariga, K.; Kunitake, T.; Lehn, J.M. Langmuir.1998, 14, 5164–5171; Bohanon, T.M.; Caruso, P.L.; Denzinger, S.; Fink, R.; Mobius, D.; Paulus, W.; Preece, J.A.; Ringsdorf, H.; Schollmeyer, D. Langmuir.1999, 15, 174–184; Hartley, J.H.; James, T.D.; Ward, C.J. J. Chem. Soc. Perkin Trans.2000, 1, 3155–3184; Pu, L. Chem. Rev.2004, 104, 1687–1716; Ludwig, R. Microchim. Acta.2005, 152, 1–19; Hembury, G.A.; Borovkov, V.V.; Inoue Y. Chem. Rev.2008, 108, 1–73; Homden, D.M.; Redshaw, C. Chem. Rev. 2008, 108, 5086–5130.
4. Stoddart, J.F. Chiral Crown Ethers. In Topics in Stereochemistry. Eliel, E.L., Wilen, S.H., Eds.; Wiley-Interscience: New York, 1988; Vol. 17, pp. 207–288. Fitzmaurice, R.J.; Kyne, G.M.; Douheret, D.; Kilburn, J.D. J. Chem. Soc. Perkin Trans. 2002, 1, 841–864; You, J.S.; Yu, X.Q.; Zhang, G.L.; Xiang, Q.X.; Lan, J.B.; Xie, R.G. Chem. Commun.2001, 1816–1817; Diederich, F. Angew. Chem., Int. Ed. Engl. 1988, 27, 362–386; Meyer, E.A.; Castellano, R.K.; Diederich, F. Angew. Chem. Int. Ed. 2003, 42, 1210–1250; Hof, F.; Craig, S.L.; Nuckolls, C.; Rebek, J., Jr. Angew. Chem. Int. Ed.2002, 41, 1488–1508; Casnati, A.; Sansone, F.; Ungaro, R. Acc. Chem. Res. 2003, 36, 246–254; de Namor, A.F.D.; Cleverley, R.M.; Zapata-Ormachea, M.L. Chem. Rev. 1998, 98, 2495–2525; Zhang, X.X.; Bradshaw, J.S.; Izatt, R.M. Chem. Rev.1997, 97, 3313–3361.
5. Chiral recognition in molecular complexing