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Volumn , Issue 21, 2010, Pages 4035-4045

Preparation of highly hindered polyenynes

Author keywords

Alkynes; Carbon rich compounds; Polyene; Polyyne hybrid compounds; Thiophenes

Indexed keywords


EID: 77954724471     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000018     Document Type: Article
Times cited : (6)

References (30)
  • 5
    • 70349697035 scopus 로고    scopus 로고
    • This study also mentions the preparation of a hexadecayne the ends of which were protected by bulky triethylsilyl groups; the characterization of this "carbon rod" (as that of 2, n = 10) rested on its UV/Vis spectra only. The largest isolated polyyne of type 2 is the decayne (2, n = 8): W. A. Chalifoux, R. McDonald, M. J. Ferguson, R. R. Tykwinski, Angew. Chem. 2009, 121, 8056-8060;
    • (2009) Angew. Chem. , vol.121 , pp. 8056-8060
    • Chalifoux, W.A.1    McDonald, R.2    Ferguson, M.J.3    Tykwinski, R.R.4
  • 6
    • 70349668793 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 7915-7919.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 7915-7919
  • 7
    • 60449114149 scopus 로고    scopus 로고
    • - For the most recent review article on conjugated polyynes, see: W. A. Chalifoux, R. R. Tykwinski, C. R. Chimie, 2009, 12, 341-358.
    • (2009) C. R. Chimie , vol.12 , pp. 341-358
    • Chalifoux, W.A.1    Tykwinski, R.R.2
  • 9
    • 33645526191 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 1034-1057.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1034-1057
  • 11
    • 77954694004 scopus 로고
    • Chem. Zbl. 1936, 1, 3347.
    • (1936) Chem. Zbl. , vol.1 , pp. 3347
  • 18
    • 33846247877 scopus 로고    scopus 로고
    • For recent reviews on the preparation of alkynes by elimination reactions, see: A. Orita, J. Otera, Chem. Rev. 2006, 106, 5387-5412;
    • (2006) Chem. Rev. , vol.106 , pp. 5387-5412
    • Orita, A.1    Otera, J.2
  • 22
    • 0001752768 scopus 로고    scopus 로고
    • Program version 5.30: F. H. Allen, Acta Cryst. B58, 380-388 (2002).
    • (2002) Acta Cryst. , vol.B58 , pp. 380-388
    • Allen, F.H.1
  • 23
    • 34250855948 scopus 로고    scopus 로고
    • see also ref. cited therein
    • - Bowed conformations have also been observed for many conjugated oligoynes in the solid state as reviewed by: S. Szafert, J. A. Gladysz, Chem. Rev. 2006, 106, PR1-PR33, see also ref. cited therein.
    • (2006) Chem. Rev. , vol.106
    • Szafert, S.1    Gladysz, J.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.