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Volumn 63, Issue 21, 1998, Pages 7286-7288

Carbonyl olefination by means of a £em-dichloride-Cp2Ti[P(OEt)3]2 system

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EID: 0000242804     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980724h     Document Type: Article
Times cited : (63)

References (42)
  • 37
    • 33744856740 scopus 로고    scopus 로고
    • note
    • 7a whereas the yield of olefination of the same ketone was largely decreased (31%) when 2,2-bis(phenylthio)butane was employed. The treatment of l,5-diphenyl-3,3-bis(phenylthio)pentane with 3 equiv of 1 at room temperature for 2 h afforded l,5-diphenyl-5-(phenylthio)pent-2-ene (44%) and the partial reduction product l,5-diphenyl-3phenylthiopentane (33%).
  • 39
    • 0001154907 scopus 로고    scopus 로고
    • 16c and trialkylsilane and related group 14 organometallics16d to produce cyclopropane, conjugated diene, γ-substituted allylsilane, and [2+l]carbenoid insertion products, respectively: (a) Horikawa, Y.; Nomura, T.; Watanabe, M.; Fujiwara, T.; Takeda, T. J. Org. Chem. 1997, 62, 3678.
    • (1997) J. Org. Chem. , vol.62 , pp. 3678
    • Horikawa, Y.1    Nomura, T.2    Watanabe, M.3    Fujiwara, T.4    Takeda, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.