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Volumn , Issue 20, 1998, Pages 3377-3379

A convenient access to iodinated calix[4]arenes

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33748513886     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a805643i     Document Type: Article
Times cited : (14)

References (60)
  • 1
    • 33748479388 scopus 로고    scopus 로고
    • Parma, Italy, Abstr. Pap. P 107
    • Presented in part at the 4th International Congress on Calixarenes, Parma, Italy, 1997, Abstr. Pap. P 107.
    • (1997) 4th International Congress on Calixarenes , Issue.PART
  • 2
    • 0003894828 scopus 로고
    • ed. J. F. Stoddart, Royal Society of Chemistry, Cambridge
    • For recent reviews on calixarenes, see: (a) C. D. Gutsche, in Monographs in Supramolecular Chemistry, ed. J. F. Stoddart, Royal Society of Chemistry, Cambridge, 1989;
    • (1989) Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
  • 7
    • 85083010444 scopus 로고
    • Functionalization of aryl iodides: E. B. Merkushev, Synthesis, 1988, 923.
    • (1988) Synthesis , pp. 923
    • Merkushev, E.B.1
  • 44
    • 33748478711 scopus 로고    scopus 로고
    • note
    • Compound 2 was previously suggested as an intermediate (see ref. 5b) without analytical verification.
  • 45
    • 33748515374 scopus 로고    scopus 로고
    • note
    • Compounds 4a and 4c were prepared by Reinhoudt et al. via the mercury salt method (see ref. 5a).
  • 46
    • 85088279376 scopus 로고    scopus 로고
    • note
    • 1H NMR data for 6 suggest a more flexible structure mainly between cone and partial-cone conformers.
  • 54
    • 0009128411 scopus 로고
    • Litwak and Biali reported the formation of spiro-calixarenes by gentle oxidation with phenyltrimethylammonium tribromide: (a) A. M. Litwak and S. E. Biali, J. Org. Chem., 1992, 57, 1943;
    • (1992) J. Org. Chem. , vol.57 , pp. 1943
    • Litwak, A.M.1    Biali, S.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.