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Volumn 48, Issue 43, 2007, Pages 7660-7664

Ullmann coupling reaction of 1,3-bistriflate esters of calix[4]arenes: facile syntheses of monoaminocalix[4]arenes and 4,4′:6,6′-diepithiobis(phenoxathiine)

Author keywords

Aminocalixarenes; Intramolecularly bridged calixarene; Ullmann coupling reaction

Indexed keywords

1,3 BISTRIFLATE ESTER; 4,4':6,6' DIEPITHIOBIS(PHENOXATHIINE); BENZYLAMINE; CALIXARENE; COPPER IODIDE; ESTER DERIVATIVE; IODINE DERIVATIVE; MONOAMINOCALIX[4]ARENE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; POTASSIUM DIHYDROGEN PHOSPHATE; UNCLASSIFIED DRUG;

EID: 34548847154     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.08.095     Document Type: Article
Times cited : (16)

References (39)
  • 1
    • 0000033877 scopus 로고
    • Calixarenes
    • Reviews:. Stoddart J.F. (Ed), The Royal Society of Chemistry, Cambridge
    • Reviews:. Gutsche C.D. Calixarenes. In: Stoddart J.F. (Ed). Monographs in Supramolecular Chemistry (1989), The Royal Society of Chemistry, Cambridge
    • (1989) Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
  • 3
    • 0003277099 scopus 로고    scopus 로고
    • Calixarenes Revisited
    • Stoddart J.F. (Ed), The Royal Society of Chemistry, Cambridge
    • Gutsche C.D. Calixarenes Revisited. In: Stoddart J.F. (Ed). Monographs in Supramolecular Chemistry (1998), The Royal Society of Chemistry, Cambridge
    • (1998) Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
  • 4
    • 0004266535 scopus 로고    scopus 로고
    • Mandolini L., and Ungaro R. (Eds), Imperial College Press, London
    • In: Mandolini L., and Ungaro R. (Eds). Calixarenes in Action (2000), Imperial College Press, London
    • (2000) Calixarenes in Action
  • 5
    • 0004287470 scopus 로고    scopus 로고
    • Asfari Z., Böhmer V., Harrowfield J.M., and Vicens J. (Eds), Kluwer Academic Publishers, Dordrecht
    • In: Asfari Z., Böhmer V., Harrowfield J.M., and Vicens J. (Eds). Calixarenes 2001 (2001), Kluwer Academic Publishers, Dordrecht
    • (2001) Calixarenes 2001
  • 6
    • 37049089386 scopus 로고
    • For transformation of the hydroxy groups of calixarenes into other functions, see:
    • For transformation of the hydroxy groups of calixarenes into other functions, see:. Goren Z., and Biali S.E. J. Chem. Soc., Perkin Trans. 1 (1990) 1484
    • (1990) J. Chem. Soc., Perkin Trans. 1 , pp. 1484
    • Goren, Z.1    Biali, S.E.2
  • 26
    • 34548827457 scopus 로고    scopus 로고
    • note
    • 6: C, 51.20; H, 4.71; S, 19.53. Found: C, 51.01; H, 4.71; S, 19.82.
  • 27
    • 34548824656 scopus 로고    scopus 로고
    • note
    • 5S: C, 71.78; H, 7.18; N, 1.61. Found: C, 71.68; H, 7.15; N, 1.48.
  • 29
    • 34548828944 scopus 로고    scopus 로고
    • note
    • 4: C, 70.13; H, 6.47; S, 18.72. Found: C, 70.11; H, 6.51; S, 18.80.
  • 37
    • 34548826894 scopus 로고    scopus 로고
    • 2e.
  • 38
    • 34548826630 scopus 로고    scopus 로고
    • note
    • 2 = 0.0754 (all data), GOF = 0.922. The details of the crystal data have been deposited with Cambridge Crystallographic Data Centre as supplementary publication No. CCDC 648696.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.