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(E)-α-Bromovinylselenides as Convenient Precursors for Stereoselective Synthesis of Trisubstituted Alkenes

(E)-α-Bromovinylselenides as Convenient Precursors for Stereoselective Synthesis of Trisubstituted Alkenes
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摘要 Based on the different reactivity of selanyl and bromo groups,( E)-α- bromovinylselenides can undergo sequential cross coupling reactions with nucleophiles in the presence of transition metal complexes to form two carbon-carbon bonds in the same olefinic carbon leading to trisubstituted alkenes stereoselectively in good yields. Based on the different reactivity of selanyl and bromo groups,( E)-α- bromovinylselenides can undergo sequential cross coupling reactions with nucleophiles in the presence of transition metal complexes to form two carbon-carbon bonds in the same olefinic carbon leading to trisubstituted alkenes stereoselectively in good yields.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2003年第11期1491-1493,共3页 中国化学(英文版)
基金 ProjectsupportedbytheNationalNaturalScienceFoundationofChina (No .2 0 0 62 0 0 2 )
关键词 (E)-α-bromovinylselenide cross coupling reaction trisubstituted alkene stereoselective synthesis (E)-α-bromovinylselenide,cross coupling reaction,trisubstituted alkene,stereoselective synthesis
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参考文献3

  • 1Coulson,D. R. Inorganic Syntheses . 1972
  • 2Venazi,L. M. J. Chemical Society Reviews . 1958
  • 3Comasseto,J. V. J.Organomet[].Chemtracts.1983

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