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Studies on Hydroiodination and Deconjugation of 5—Aryloxy—(thiophenyl)—3—pentyn—2—one
引用本文:刘利军,罗芬台.Studies on Hydroiodination and Deconjugation of 5—Aryloxy—(thiophenyl)—3—pentyn—2—one[J].中国化学,2002,20(9):895-898.
作者姓名:刘利军  罗芬台
作者单位:[1]DepartmentofChemistryandTechnology,NingxiaUniversity,Yinchuan,Ningxia750001,China [2]InstituteofChemistry,AcademiaSinica,Taipei,TaiwanSheng11529,China
基金项目:theScienceCouncilandAcademiaSinicaofTaiwan China
摘    要: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 plasuible 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.

关 键 词:5-芳氧基-(硫苯基)-3-戊炔-2-酮  碘氢化反应  β-取代  理论研究

Studies on Hydroiodination and Deconjugation of 5-Aryloxy-(thiophenyl)-3-pentyn-2-one
Li‐Jun Liu,Fen‐Tair Luo.Studies on Hydroiodination and Deconjugation of 5-Aryloxy-(thiophenyl)-3-pentyn-2-one[J].Chinese Journal of Chemistry,2002,20(9):895-898.
Authors:Li‐Jun Liu  Fen‐Tair Luo
Abstract: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 °C 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.
Keywords:β‐substituted β  γ‐enone  hydroiodination  deconjugation
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