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Volumn 46, Issue 1, 2005, Pages 27-30

Synthesis of organosilicon polymers by using the Lewis-acid-catalyzed trans-allylsilylation of alkynes

Author keywords

Conjugation; Allylsilylation; Carbometallation; Hafnium chloride; Lewis acid catalyst; Organosilicon polymer

Indexed keywords

ALKYNE DERIVATIVE; CHLORINE DERIVATIVE; LEWIS ACID; ORGANOSILICON DERIVATIVE; SILANE DERIVATIVE;

EID: 9944246067     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.11.048     Document Type: Article
Times cited : (12)

References (40)
  • 1
    • 0003290223 scopus 로고
    • Inorganic and Organometallic Polymers
    • American Chemical Society Washington, DC
    • M. Zeldin, K.J. Wynne, and H.R. Allcock Inorganic and Organometallic Polymers ACS Symposium Series Vol. 368 1988 American Chemical Society Washington, DC
    • (1988) ACS Symposium Series , vol.368
    • Zeldin, M.1    Wynne, K.J.2    Allcock, H.R.3
  • 2
    • 0000133662 scopus 로고
    • Silicon-Based Polymer Science
    • American Chemical Society Washington, DC
    • J.M. Zeigler, and F.W.G. Fearon Silicon-Based Polymer Science Advances in Chemistry Series Vol. 224 1990 American Chemical Society Washington, DC
    • (1990) Advances in Chemistry Series , vol.224
    • Zeigler, J.M.1    Fearon, F.W.G.2
  • 16
    • 0001522634 scopus 로고
    • B.M. Trost I. Fleming Pergamon Oxford
    • For reviews, see: P. Knochel B.M. Trost I. Fleming Comprehensive Organic Synthesis Vol. 4 1991 Pergamon Oxford 865 911
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 865-911
    • Knochel, P.1
  • 20
    • 9944252699 scopus 로고    scopus 로고
    • note
    • 3) δ 156.7, 143.9, 136.0, 128.0, 127.7, 126.9, 126.5, 116.2, 47.0, -1.9, -2.6
  • 21
    • 9944263239 scopus 로고    scopus 로고
    • note
    • 3) δ 157.3, 143.9, 135.8, 127.88, 127.86, 127.7, 126.9, 116.4, 46.8, 0.1
  • 23
    • 9944232862 scopus 로고    scopus 로고
    • note
    • max/nm (ε) 252 nm (12,000)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.