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Double Nucleophilic Addition of Ketene Silyl (THIO)Acetals and Trimethylsilyl Cyanide to N-Allylideneamine

Double Nucleophilic Addition of Ketene Silyl (THIO)Acetals and Trimethylsilyl Cyanide to N-Allylideneamine
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摘要 1 Results We have already published a double nucleophilic addition reaction of α,β-unsaturated imines with several nucleophiles such as ketene silyl acetals, trimethylsilyl cyanides, trimethylsilyl azides and thiols[1]. However, it was not easy to use N-allylideneamine 2 derived from acrolein for such reactions. Since there is no substituent at the β-position, imine 2 has high reactivity and are prone to be polymerization. We report the first synthesis of N-allylideneamines 2 using the isomerization of ...
出处 《复旦学报(自然科学版)》 CAS CSCD 北大核心 2007年第5期586-,共1页 Journal of Fudan University:Natural Science
关键词 double nucleophilic addition reaction regioselectivity N-allylideneamine silica gel ketene silyl acetal double nucleophilic addition reaction regioselectivity N-allylideneamine silica gel ketene silyl acetal
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参考文献4

  • 1MShi mizu,A Takahashi,S Kawai. Organic Letters . 2006
  • 2M Shi mizu,A Morita,T Kaga. Tetrahedron Letters . 1999
  • 3M Shi mizu,M Kamiya,I Hachiya. Chem Lett . 2003
  • 4MShi mizu,M Kamiya,I Hachiya. Chemistry Letters . 2005

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