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Volumn 9, Issue 12, 2007, Pages 2393-2396

Intramolecular SNAr reactions in a large-ring Ketocalix[6]arene

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EID: 34347271003     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol070870m     Document Type: Article
Times cited : (21)

References (31)
  • 1
    • 0004268367 scopus 로고    scopus 로고
    • For reviews on calixarenes, see: a, Royal Society of Chemistry: Cambridge
    • For reviews on calixarenes, see: (a) Gutsche, C. D. Calixarenes Revisited; Royal Society of Chemistry: Cambridge, 1998.
    • (1998) Calixarenes Revisited
    • Gutsche, C.D.1
  • 2
    • 0004287470 scopus 로고    scopus 로고
    • Asfari, Z, Böhmer, V, Harrowfield, J, Vicens, J, Eds, Kluwer Academic Publishers: Dordrecht
    • (b) Calixarenes 2001; Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer Academic Publishers: Dordrecht, 2001.
    • (2001) Calixarenes 2001
  • 3
    • 0345736841 scopus 로고    scopus 로고
    • Rappoport, Z, Ed, Wiley: Chichester, Chapter 19
    • (c) Böhmer, V. In The Chemistry of Phenols; Rappoport, Z., Ed.; Wiley: Chichester, 2003; Chapter 19.
    • (2003) The Chemistry of Phenols
    • Böhmer, V.1
  • 9
    • 0037244554 scopus 로고    scopus 로고
    • For a review on spirodienone calixarene derivatives, see
    • For a review on spirodienone calixarene derivatives, see: Biali, S. E. Synlett 2003, 1.
    • (2003) Synlett , pp. 1
    • Biali, S.E.1
  • 13
    • 0003110217 scopus 로고    scopus 로고
    • For a review on the oxidation and reduction of calixarenes, see:, Asfari, Z, Böhmer, V, Harrowfield, J, Vicens, J, Eds, Kluwer Academic Publishers: Dordrecht
    • For a review on the oxidation and reduction of calixarenes, see: Biali, S. E. In Calixarenes 2001; Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer Academic Publishers: Dordrecht, 2001; p 266.
    • (2001) Calixarenes 2001 , pp. 266
    • Biali, S.E.1
  • 17
    • 34347214354 scopus 로고    scopus 로고
    • Ketocalixarenes possessing a single carbonyl bridge were synthesized by Sone and co-workers by a stepwise route. See: Ito, K, Izawa, S, Ohba, T, Ohba, Y, Sone, T. Tetrahedron Lett. 1996, 37, 5959
    • Ketocalixarenes possessing a single carbonyl bridge were synthesized by Sone and co-workers by a stepwise route. See: Ito, K.; Izawa, S.; Ohba, T.; Ohba, Y.; Sone, T. Tetrahedron Lett. 1996, 37, 5959.
  • 18
    • 0035977622 scopus 로고    scopus 로고
    • Such a synthetic strategy was introduced by Miyano and co-workers who reported the replacement of the methoxy groups of oxidized thiacalixarenes by amino groups. See: Katagiri, H, Iki, N, Hattori, T, Kabuto, C, Miyano, S. J. Am. Chem. Soc. 2001, 123, 779
    • Such a synthetic strategy was introduced by Miyano and co-workers who reported the replacement of the methoxy groups of oxidized thiacalixarenes by amino groups. See: Katagiri, H.; Iki, N.; Hattori, T.; Kabuto, C.; Miyano, S. J. Am. Chem. Soc. 2001, 123, 779.
  • 27
    • 34347237727 scopus 로고    scopus 로고
    • Compound 6 was identified on the basis of its NMR spectrum in the crude product mixture and was not isolated in pure form.
    • Compound 6 was identified on the basis of its NMR spectrum in the crude product mixture and was not isolated in pure form.


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