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Volumn , Issue 2, 2009, Pages 223-237

Paracyclophanes: Extending the bridges. Synthesis

Author keywords

m.n paracyclophanes; Cyclophanes; Ring contraction; Sulfone pyrolysis; Thiacyclophanes

Indexed keywords


EID: 58649094192     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200800494     Document Type: Article
Times cited : (21)

References (49)
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    • P. M. Keehn, S. M. Rosenfeld Eds, Academic Press
    • b) P. M. Keehn, S. M. Rosenfeld (Eds.) Cyclophanes, vol. I and II, Academic Press, 1983;
    • (1983) Cyclophanes , vol.I and II
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    • 0003825877 scopus 로고
    • The Royal Society of Chemistry, Cambridge
    • c) F. Diederich, Cyclophanes, The Royal Society of Chemistry, Cambridge, 1991;
    • (1991) Cyclophanes
    • Diederich, F.1
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    • H. Takemura Ed, Research Signpost, Trivandrum
    • st Century, Research Signpost, Trivandrum, 2002;
    • (2002) st Century
  • 8
    • 3242887372 scopus 로고    scopus 로고
    • R. Gleiter, H. Hopf Eds, Wiley-VCH, Weinheim
    • e) R. Gleiter, H. Hopf (Eds.), Modern Cyclophane Chemistry, Wiley-VCH, Weinheim, 2004.
    • (2004) Modern Cyclophane Chemistry
  • 9
    • 58649102103 scopus 로고    scopus 로고
    • In the Table in Scheme 1 the references given only refer to leading references, i.e. the Table does not try to be a complete reflection of the vast chemical literature; see ref.[4] for the review literature in this field. The Table begins with the lowest possible [m.n]paracyclophane and ends with the [4.4]hydrocarbon, since beyond this limit the phanes are beginning to lose the characteristic deformations and rigidity that are so typical of the lower members of the series
    • In the Table in Scheme 1 the references given only refer to leading references, i.e. the Table does not try to be a complete reflection of the vast chemical literature; see ref.[4] for the review literature in this field. The Table begins with the lowest possible [m.n]paracyclophane and ends with the [4.4]hydrocarbon, since beyond this limit the phanes are beginning to lose the characteristic deformations and rigidity that are so typical of the lower members of the series.
  • 11
    • 58649083957 scopus 로고    scopus 로고
    • For a recent summary on the preparation of [n]- and [m.n]cyclophanes see H. Hopf in Beyond van't Hoff and LeBel (Ed.: H. Dodziuk), Wiley-VCH, Weinheim, 2008, in print.
    • For a recent summary on the preparation of [n]- and [m.n]cyclophanes see H. Hopf in Beyond van't Hoff and LeBel (Ed.: H. Dodziuk), Wiley-VCH, Weinheim, 2008, in print.
  • 14
    • 0343440750 scopus 로고    scopus 로고
    • For the preparation of derivatives of [1.4]paracyclophane as well as higher homologs see: a H. A. Staab, A. Ruland, C. Kuo-chen, Chem. Ber. 1982, 115, 1755-1764;
    • For the preparation of derivatives of [1.4]paracyclophane as well as higher homologs see: a) H. A. Staab, A. Ruland, C. Kuo-chen, Chem. Ber. 1982, 115, 1755-1764;
  • 34
    • 4244143012 scopus 로고
    • and references to earlier literature
    • J. Grütze, F. Vögtle, Chem. Ber. 1977, 110, 1978-1993 and references to earlier literature.
    • (1977) Chem. Ber , vol.110 , pp. 1978-1993
    • Grütze, J.1    Vögtle, F.2
  • 41
    • 58649083060 scopus 로고    scopus 로고
    • Prepared from the dibromide 13 as described in the Exp. Section.
    • Prepared from the dibromide 13 as described in the Exp. Section.
  • 42
    • 0000832331 scopus 로고    scopus 로고
    • 8][3.3]paracyclophane.
    • 8][3.3]paracyclophane.
  • 43
    • 0000979629 scopus 로고    scopus 로고
    • 4][3.3]paracyclophane.
    • 4][3.3]paracyclophane.
  • 44
    • 58649101167 scopus 로고    scopus 로고
    • Several of the intermediates described below have been described in the chemical literature. However, since the experimental details are often incomplete and spectroscopic data missing we briefly repeat the syntheses of these compounds here
    • Several of the intermediates described below have been described in the chemical literature. However, since the experimental details are often incomplete and spectroscopic data missing we briefly repeat the syntheses of these compounds here.
  • 48


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.