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Volumn 52, Issue 12, 2011, Pages 1351-1353

Synthesis of BINOL-containing oxacalix[4]arenes

Author keywords

BINOL; Chiral heteracalixarenes; Oxacalixarenes

Indexed keywords

1,5 DIFLUORO 2,4 DINITROBENZENE; 2,2' DIHYDROXY 1,1' BINAPHTHYL; CALIXARENE; NITROBENZENE; OXACALIX[4]ARENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79951754044     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.01.061     Document Type: Article
Times cited : (17)

References (58)
  • 1
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    • Calixarenes - An Introduction
    • 2nd ed. Stoddart, J. F., Ed.; The Royal Society of Chemistry: Cambridge, UK
    • Gutsche, C. D. Calixarenes - An Introduction, 2nd ed. In Monographs in Supramolecular Chemistry; Stoddart, J. F., Ed.; The Royal Society of Chemistry: Cambridge, UK, 2008; Vol. 6.
    • (2008) Monographs in Supramolecular Chemistry , vol.6
    • Gutsche, C.D.1
  • 7
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    • Katritzky, A. R., Ramsden, C. A., Scriven, E. F. V., Taylor, R. J. K., Eds.; Elsevier: Oxford, UK
    • (b) Parisi, M. F.; Pappalardo, S. In Comprehensive Heterocyclic Chemistry III; Katritzky, A. R., Ramsden, C. A., Scriven, E. F. V., Taylor, R. J. K., Eds.; Elsevier: Oxford, UK, 2008; Vol. 14, pp 667-750.
    • (2008) Comprehensive Heterocyclic Chemistry III , vol.14 , pp. 667-750
    • Parisi, M.F.1    Pappalardo, S.2
  • 39
  • 40
    • 0000718373 scopus 로고    scopus 로고
    • (b) Pu, L. Chem. Rev. 1998, 98, 2405-2494;
    • (1998) Chem. Rev. , vol.98 , pp. 2405-2494
    • Pu, L.1
  • 41
    • 64149120940 scopus 로고    scopus 로고
    • For some relevant examples of BINOL-containing 'classical' calixarenes, see: (c)
    • For some relevant examples of BINOL-containing 'classical' calixarenes, see: (c) Shirakawa, S.; Shimizu, S. Eur. J. Org. Chem. 2009, 1916-1924;
    • (2009) Eur. J. Org. Chem. , pp. 1916-1924
    • Shirakawa, S.1    Shimizu, S.2
  • 45
    • 79951745979 scopus 로고    scopus 로고
    • note
    • 12: C, 69.33; H, 3.13; N, 6.22. Found: C, 68.97; H, 3.26; N, 6.14.
  • 46
    • 79951755625 scopus 로고    scopus 로고
    • note
    • int = 0.0621) out of 247,629 collected, R1 = 0.0494 and wR2 = 0.1269 and GoF = 0.941 for 6026 reflections with I > 2σ(I). Detailed information on crystal data and model refinement can be found in Table S1 (Supplementary data). Crystallographic data for (R,S)-1 (excluding structure factors) have been deposited with the Cambridge Crystallographic Data Centre as the supplementary publication no. CCDC 801761. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK, (fax: +44 (0)1223 336033 or e-mail: deposit@ccdc.cam.ac.uk).
  • 47
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    • Newman, M. S., Ed.; John Wiley and Sons: New York, Chapter 12
    • (a) Westheimer, F. H. In Steric Effects in Organic Chemistry; Newman, M. S., Ed.; John Wiley and Sons: New York, 1956. Chapter 12;
    • (1956) Steric Effects in Organic Chemistry
    • Westheimer, F.H.1
  • 54
    • 79951753915 scopus 로고    scopus 로고
    • note
    • 3).
  • 58
    • 0000671730 scopus 로고    scopus 로고
    • Aromatic transetherification, catalyzed by nucleophiles (such as fluoride ions), is a reversible process that has been used in dynamic covalent chemistry. For a review, see
    • Aromatic transetherification, catalyzed by nucleophiles (such as fluoride ions), is a reversible process that has been used in dynamic covalent chemistry. For a review, see: Rowan, S. J.; Cantrill, S. J.; Cousins, G. R. L.; Sanders, J. K. M.; Stoddart, J. F. Angew. Chem., Int. Ed. 2002, 41, 898-952.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 898-952
    • Rowan, S.J.1    Cantrill, S.J.2    Cousins, G.R.L.3    Sanders, J.K.M.4    Stoddart, J.F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.