[2,3]-Wittig rearrangement of methyl β-pyrrolidinyl-γ-allyloxy-(E)-2-butenoate. Expeditious synthesis of 5-alkenyl-4-pyrrolidin-1-yl-5H-furan-2-ones |
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Authors: | Yu-Jang Li Pei-Ting Lee Yuan-Kang Chang Yi-Hung Liu |
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Institution: | a Department of Applied Chemistry, National Chiayi University, Chiayi 600, Taiwan, ROC b Department of Applied Chemistry, Chaoyang University of Technology, Wufeng 413, Taichung county, Taiwan, ROC c Department of Chemistry, National Taiwan University, Taipei 106, Taiwan, ROC |
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Abstract: | Dienolates of various γ-allyloxy substituted methyl β-pyrrolidinyl (E)-2-butenoate undergo a 2,3]-Wittig rearrangement to generate various 5-alkenyl-4-pyrrolidin-1-yl-5H-furan-2-one type compounds. |
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Keywords: | [2 3]-Wittig rearrangement |
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