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Volumn , Issue 11, 1997, Pages 2315-2320

Calixarene carbamates

Author keywords

Calixarenes; Macrocyclic ligands; Molecular modelling; Molecular recognition; Supramolecular chemistry

Indexed keywords


EID: 33748721951     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719971120     Document Type: Article
Times cited : (6)

References (54)
  • 6
    • 33748720311 scopus 로고
    • A. D. Hamilton (Ed.), Symposia in print No. 56
    • [1f] A. D. Hamilton (Ed.), Molecular Recognition, Tetrahedron, Symposia in print No. 56, 1995, 51.
    • (1995) Molecular Recognition, Tetrahedron , vol.51
  • 11
    • 0003894828 scopus 로고
    • (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge
    • [2a] For the description of calix[4]arene conformations see: C. D. Gutsche, Calixarenes in Monographs in Supramolecular Chemistry (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1992.
    • (1992) Calixarenes in Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
  • 18
    • 0000334793 scopus 로고
    • [3c] R. Ungaro, Angew. Chem. 1994, 106, 1551-1553;
    • (1994) Angew. Chem. , vol.106 , pp. 1551-1553
    • Ungaro, R.1
  • 23
  • 24
    • 0001670792 scopus 로고    scopus 로고
    • J. L. Atwood, J. E. D. Davies, D. D. Macnicol, F. Vögtle, J.-M. Lehn, Eds., Pergamon, Oxford, UK
    • [4e] A. Pochini, R. Ungaro, in Comprehensive Supramolecular Chemistry (J. L. Atwood, J. E. D. Davies, D. D. Macnicol, F. Vögtle, J.-M. Lehn, Eds.), Vol. 2, Pergamon, Oxford, UK, 103-142.
    • Comprehensive Supramolecular Chemistry , vol.2 , pp. 103-142
    • Pochini, A.1    Ungaro, R.2
  • 29
    • 33748734970 scopus 로고    scopus 로고
    • note
    • 2 has been used for the selective triple acylation of tetrahydroxy-para-tert-butyl calix[4]arene. However, this base was not suitable for a selective acylation with n-butyl isocyanate.
  • 35
    • 33748716265 scopus 로고    scopus 로고
    • Triply acylated calixarenes have been isolated in small yields from the reaction with acyl chlorides. See ref.[5]
    • [7f] Triply acylated calixarenes have been isolated in small yields from the reaction with acyl chlorides. See ref.[5]
  • 36
    • 0000424340 scopus 로고    scopus 로고
    • J. L. Atwood, J. E. D. Davies, D. D. Macnicol, F. Voatle, J.-M. Lehn, Eds., Pergamon, Oxford, UK
    • [8a] Several calixarene amides are strong ionophores. M. A. McKervey, M.-J. Schwing-Weill, F. Arnaud-Neu in Comprehensive Supramolecular Chemistry (J. L. Atwood, J. E. D. Davies, D. D. Macnicol, F. Voatle, J.-M. Lehn, Eds.), Vol. 1, Pergamon, Oxford, UK, 1996, pp. 537-603.
    • (1996) Comprehensive Supramolecular Chemistry , vol.1 , pp. 537-603
    • McKervey, M.A.1    Schwing-Weill, M.-J.2    Arnaud-Neu, F.3
  • 37
    • 33748716948 scopus 로고    scopus 로고
    • note
    • [8b] The cocrystallisation of 1 and 3 with alkalimetal salts under various conditions were not successful.
  • 38
    • 0001937784 scopus 로고    scopus 로고
    • (Eds.: J.-M. Lehn, J. L. Atwood, J. E. D. Davies, D. D. Macnicol, F. Vögtle, D. N. Reinhoudt), Pergamon, Oxford
    • For reviews of this topic, see: (9a] F. de Jong, H. C. Visser, in Comprehensive Supramolecular Chemistry, Vo.l 10 (Eds.: J.-M. Lehn, J. L. Atwood, J. E. D. Davies, D. D. Macnicol, F. Vögtle, D. N. Reinhoudt), Pergamon, Oxford, 1996, pp. 13-51.
    • (1996) Comprehensive Supramolecular Chemistry, Vo.l 10 , vol.10 , pp. 13-51
    • De Jong, F.1    Visser, H.C.2
  • 44
    • 33748737069 scopus 로고    scopus 로고
    • unpublished results
    • [10a] In competitive salt extraction experiments or ion transport experiments a source phase containing several nitrate salts is used. The salt content of the receiving phase (or the extracted aqueous phase) is analyzed by inductively coupled plasma atom emission spectroscopy (ICP-AES). This procedure allows the investigation of the transport pattern of a compound under given conditions in a single experiment. B. König, M. Bahadir, M. Müller, H. Wichman, unpublished results.
    • König, B.1    Bahadir, M.2    Müller, M.3    Wichman, H.4
  • 47
    • 33748733739 scopus 로고    scopus 로고
    • note
    • As in the case of the smaller calixarene carbamates, 6 and 7 show intensive molecular ions of their alkali metal complexes in mass spectra. Their transport ability was tested in membrane transport of metal salts giving no significant activity.
  • 48
    • 0001788260 scopus 로고    scopus 로고
    • A solution of 3 in acetone was refluxed to investigate a possible catalysis of the aldol reaction under neutral conditions. However, GC analysis showed that no additional aldol addition product was formed under these conditions. For a recent example of the use of calixarenes as catalysts see: N. Pirrincioglu, F. Zaman, A. Williams, J. Chem. Soc., Perkin Trans. 2 1996, 2561-2562.
    • (1996) J. Chem. Soc., Perkin Trans. 2 , pp. 2561-2562
    • Pirrincioglu, N.1    Zaman, F.2    Williams, A.3
  • 49
    • 33748739784 scopus 로고    scopus 로고
    • note
    • -1.
  • 50
    • 33748720310 scopus 로고    scopus 로고
    • note
    • The calculations were performed independently without the use of experimental data.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.