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Chiral Calixarenes Functionalized with Camphorsulfonyl Groups. Synthesis, Structure and Inclusion Properties

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Molecular Recognition and Inclusion

Abstract

The interest for calixarenes is now well established in the field of supramolecular chemistry and in the synthesis of host compounds for ions and neutral molecules. The development of chiral calixarenes is an important step for the evolution of these macrocycles if we consider a possible enantioselective recognition or discrimination. The chirality in calixarenes can be obtained by several approaches1,2,3.

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References

  1. Muthukrishanan, R.; Gutsche, C.D.(1979) J. Org. Chem, 44, 3962.

    Article  Google Scholar 

  2. Böhmer, V.; Marschollek, F.; Zetta, L.(1987) J. Org. Chem., 52, 3200.

    Article  Google Scholar 

  3. Pappalardo, S.; Caccamese, S.; Giunta, L. (1991) Tet.Lett., 52, 7747.

    Article  Google Scholar 

  4. Main, P., Hull, S.E., Leisinger, L., Germain, G., Decercq, J.P., Woolfson, M.M. (1980) Multan 80. A system of computer program for automatic solution of crystal studies from X-Ray diffraction data, Univ. of York, England and Univ. of Louvain, Belgique.

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  5. Sheldrick, G.M. (1976) Shelx, Program for Crystal Structure determination, Univ. of Cambridge, England.

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  6. Sheldrick, G.M.; Shelxl (1993) Univ.of Göttingen, Germany.

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  7. Bavoux, C.; Perrin, M.; Chino, P. (1994) Supramol. Chem, 4, 63.

    Article  CAS  Google Scholar 

  8. Motta, L.; Regnouf De Vains, J.B.; Bavoux, C.; Perrin, M.(1995) J. Chem. Crysu 7, 401.

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© 1998 Springer Science+Business Media Dordrecht

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Viola, L.M., Regnouf de Vains, JB., Bavoux, C., Perrin, M. (1998). Chiral Calixarenes Functionalized with Camphorsulfonyl Groups. Synthesis, Structure and Inclusion Properties. In: Coleman, A.W. (eds) Molecular Recognition and Inclusion. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-5288-4_75

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  • DOI: https://doi.org/10.1007/978-94-011-5288-4_75

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-6226-8

  • Online ISBN: 978-94-011-5288-4

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