| 氮杂环丙烷与腈的[3+2]环加成反应生成咪唑啉的研究进展 |
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| 引用本文： | 魏文珑,杨学绮,李兴,常宏宏.氮杂环丙烷与腈的[3+2]环加成反应生成咪唑啉的研究进展[J].化工时刊,2011,25(3):44-47. |
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| 作者姓名： | 魏文珑 杨学绮 李兴 常宏宏 |
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| 作者单位： | 太原理工大学化学化工学院,山西,太原,030024 |
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| 摘 要： | 咪唑啉是一种非常重要的药物中间体,其通过氮杂环丙烷与腈的3+2]环加成反应是非常有效合成方法.综述了这种方法的研究进展,并且进行了评价与展望.
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| 关 键 词： | 咪唑啉 氮杂环丙烷 [3+2]环加成反应 合成方法 综述 |
Advance in Synthesis of Imidazoline by [3+2] -Cycloaddition of N-tosyl Aziridines with nitriles |
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| Wei Wenlong,Yang Xueqi,Chang Honghong,Li Xing.Advance in Synthesis of Imidazoline by [3+2] -Cycloaddition of N-tosyl Aziridines with nitriles[J].Chemical Industry Times,2011,25(3):44-47. |
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| Authors: | Wei Wenlong Yang Xueqi Chang Honghong Li Xing |
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| Affiliation: | Wei Wenlong Yang Xueqi Chang Honghong Li Xing(College of Chemistry and Chemical Engineering;Taiyuan University of Technology;Shanxi Taiyuan 030024) |
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| Abstract: | Imidazolines are useful intermediates for the preparation of drugs and relevant compounds,which are synthetized by 3+2]-Cycloaddition of various substituted N-tosyl aziridines with nitriles as a quite efficient method.The research progress of this method was reviewed、evaluated and prospected. |
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| Keywords: | Imidazolines N-tosyl aziridines [3+2]-cycloaddition synthetic method |
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