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Volumn 2, Issue 16, 2000, Pages 2471-2473

The first electrochemically active cuppedophanes: Bis(tetrathiafulvalene)cuppedophanes

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EID: 0042409535     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol000138m     Document Type: Article
Times cited : (5)

References (28)
  • 4
    • 0003352208 scopus 로고
    • Cyclophanes
    • Stoddart, F. J., Ed.; The Royal Society of Chemistry: London
    • Diederich, F. Cyclophanes. Monographs in Supramolecular Chemists; Stoddart, F. J., Ed.; The Royal Society of Chemistry: London, 1991.
    • (1991) Monographs in Supramolecular Chemists
    • Diederich, F.1
  • 18
    • 0001287786 scopus 로고
    • A number of so-called double-bridged bis(tetrathiafulvaleno)phanes, connected in a 2,3-2′,3′ fashion by two linkers have been reported, see: (a) Otsubo, T.; Ogura, F. Bull. Chem. Soc. Jpn. 1985, 58, 1343-1344.
    • (1985) Bull. Chem. Soc. Jpn. , vol.58 , pp. 1343-1344
    • Otsubo, T.1    Ogura, F.2
  • 27
    • 0002331201 scopus 로고    scopus 로고
    • and references therein
    • For the deprotection-realkylation protocol using the cyanoethyl thiolate protecting group, see: Simonsen, K. B.; Becher, J. Synlett 1997, 1211-1220, and references therein.
    • (1997) Synlett , pp. 1211-1220
    • Simonsen, K.B.1    Becher, J.2
  • 28
    • 0041877952 scopus 로고    scopus 로고
    • note
    • 16 (1211.9): C, 49.56; H, 3.49; N, 4.62; S, 42.33. Found: C, 49.38; H, 3.49; N, 4.57; S, 42.17.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.