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Volumn 47, Issue 49, 2006, Pages 8689-8692

BBr3-promoted cyclization to produce ladder-type conjugated polymer

Author keywords

[No Author keywords available]

Indexed keywords

BORON TRIBROMIDE; POLYMER;

EID: 33750472722     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.10.020     Document Type: Article
Times cited : (18)

References (26)
  • 19
    • 0017777741 scopus 로고
    • 3-promoted cyclization was used to prepare 5- or 6-membered ring in the synthesis of Vernolepin and Vernomenin.
    • 3-promoted cyclization was used to prepare 5- or 6-membered ring in the synthesis of Vernolepin and Vernomenin. Grieco P.A., Nishizawa M., Oguri T., Burke S.D., and Marinovic N. J. Am. Chem. Soc. 99 (1977) 5773
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 5773
    • Grieco, P.A.1    Nishizawa, M.2    Oguri, T.3    Burke, S.D.4    Marinovic, N.5
  • 20
    • 33750444751 scopus 로고    scopus 로고
    • note
    • 1/c space group. Crystallographic data in CIF format for the structure reported here have been deposited at the Cambridge Crystallographic Data Centre (Deposition No. CCDC-617985). Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [e-mail: deposit@ccdc.cam.ac.uk].
  • 21
    • 33750484149 scopus 로고    scopus 로고
    • note
    • The crystal data, together with the refined atomic coordinates and anisotropic thermal parameters, for 1a and experimental procedures for the syntheses of all compounds are available in the Supplementary data.
  • 22
    • 33750475373 scopus 로고    scopus 로고
    • note
    • max = 433 nm in dichloromethane. It should be also mentioned that a large Stokes shift was observed for 1a despite its rigid planar structure, and there are no rational explanations on this at the current state.
  • 23
    • 33750476474 scopus 로고    scopus 로고
    • note
    • 4, respectively.
  • 24
    • 33750436401 scopus 로고    scopus 로고
    • note
    • Synthesis of the compound 5 requires the conversion of the corresponding benzyl alcohol to the benzyl chloride as direct cross-coupling reaction using benzyl chloride gave the product in low yield (10%). See Supplementary data for details.
  • 25
    • 33750454621 scopus 로고    scopus 로고
    • Bruker, SMART and SAINT: Area Detector Control and Integration Software Ver. 5.0, Bruker Analytical X-ray Instruments: Madison, Wisconsin, 1998.
  • 26
    • 33750429082 scopus 로고    scopus 로고
    • Bruker; shextl: Structure Determination Programs Ver. 5.16, Bruker Analytical X-ray Instruments: Madison, Wisconsin, 1998.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.