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A Convenient Synthesis of 2-Aryl-3-per(poly)fluoroacylindoles

A Convenient Synthesis of 2-Aryl-3-per(poly)fluoroacylindoles
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摘要 2-Aryl-3-per(poly) fluoroacylindoles were synthesized in good yields by the 1,3-dipolar cycloaddition reaction of C-aryl-N-phenylnitrones with fluorine-containing olefins and the subsequent rearrangement of the adducts. An ionic mechanism was proposed for the formation of the titled compounds. 2-Aryl-3-per(poly) fluoroacylindoles were synthesized in good yields by the 1,3-dipolar cycloaddition reaction of C-aryl-N-phenylnitrones with fluorine-containing olefins and the subsequent rearrangement of the adducts. An ionic mechanism was proposed for the formation of the titled compounds.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2002年第11期1330-1333,1130,共4页 中国化学(英文版)
基金 theNationalNaturalScienceFoundationofChina (Nos.2 990 2 0 0 8and 2 0 172 0 6 5 )
关键词 1 3-dipolar cycloaddition REARRANGEMENT fluorine-containing indole 1,3-dipolar cycloaddition rearrangement fluorine-containing indole
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参考文献10

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