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L-苯丙氨酸与β,γ-不饱和酮酸酯的[3+2]环加成反应

L-phenylalanine and β,γ-Unsaturated Keto Esters of [3+2] Cycloaddition
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摘要 运用简单的L-苯丙氨酸与β,γ-不饱和酮酸酯的[3+2]环加成反应合成吡咯衍生物,在80℃条件下能取得最好68%的产率,达到2∶1的区域选择性,合成了8个未见文献报道的取代的吡咯衍生物,其结构得到1H NMR,HRMS确证. The L-phenylalanine and fl, T-unsaturated ketone acid ester of [ 3 + 2 ] cycloaddition reaction , at 80℃ can get 68% yield and 2:1 regioselectivity. In this paper , we have synthesized 8 derivatives of tile piperidines,and its structures were confirmated by 1H NMR , HRMS.
出处 《西华师范大学学报(自然科学版)》 2013年第1期45-48,共4页 Journal of China West Normal University(Natural Sciences)
基金 国家自然科学基金(20772097)资助项目
关键词 [3+2]环加成 β γ-不饱和酮酸酯 L-苯丙氨酸 [ 3 + 2 ] cycloadditio β,γ-unsaturated ketone acid ester L-phenylalanine
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