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Studies on Hydroiodination and Deconjugation of 5-Aryloxy-(thiophenyl)-3-pentyn-2-one 被引量:1

Studies on Hydroiodination and Deconjugation of 5-Aryloxy-(thiophenyl)-3-pentyn-2-one
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摘要 b Institute of Chemistry, Academia Sinica, Taipei, Taiwan 11529, China One pot hydroiodination and deconjugation of 5 aryloxy(or thiophenyl) 3 pentyn 2 one with a reagent system of sodium iodide/trimethylsilyl chloride/water in acetonitrile at 25 ℃ have been described. The plausible mechanism was discussed. The reaction provided a simple and useful method for the preparation of ( Z ) β substituted β,γ enones and ( Z ) β substituted α,β unsaturated ketones. b Institute of Chemistry, Academia Sinica, Taipei, Taiwan 11529, China One pot hydroiodination and deconjugation of 5 aryloxy(or thiophenyl) 3 pentyn 2 one with a reagent system of sodium iodide/trimethylsilyl chloride/water in acetonitrile at 25 ℃ have been described. The plausible mechanism was discussed. The reaction provided a simple and useful method for the preparation of ( Z ) β substituted β,γ enones and ( Z ) β substituted α,β unsaturated ketones.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2002年第9期895-898,共4页 中国化学(英文版)
基金 theScienceCouncilandAcademiaSinicaofTaiwan China
关键词 substituted β γ enone hydroiodination deconjugation substituted β,γ enone, hydroiodination, deconjugation
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  • 1Ma S,Gao W.Efficient synthesis of 2,3-dihydrofurans via the highly selective Pd(0)-catalyzed coupling-cyclization reaction of 3,4-allenols with aryl iodides[J].Syn Lett,2002,1:65-68.
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