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An efficient synthesis of 2,3-diaryl-2-azabicyclo[2.2.2]octan-5-ones and their acetylcholinesterase inhibitory activity 被引量:1

An efficient synthesis of 2,3-diaryl-2-azabicyclo[2.2.2]octan-5-ones and their acetylcholinesterase inhibitory activity
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摘要 A series of substituted 2,3-diaryl-2-azabicyclo[2.2.2]octan-5-ones have been prepared by an efficient three-component aza-Diels-Alder cycloaddition reaction in water catalyzed by layered α-zirconium hydrogen phosphate (α-ZrP) and sodium calix[4]arene sulfonates bearing pendant short aliphatic chains. The 18 synthesized compounds were assayed for acetylcholinesterase inhibition using mouse acetvlcho]inesterase. A series of substituted 2,3-diaryl-2-azabicyclo[2.2.2]octan-5-ones have been prepared by an efficient three-component aza-Diels-Alder cycloaddition reaction in water catalyzed by layered α-zirconium hydrogen phosphate (α-ZrP) and sodium calix[4]arene sulfonates bearing pendant short aliphatic chains. The 18 synthesized compounds were assayed for acetylcholinesterase inhibition using mouse acetvlcho]inesterase.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2013年第4期347-350,共4页 中国化学快报(英文版)
基金 financial support from the Natural Science Foundation of China(No.21176222)
关键词 Aza-Diels-Alder cycloadditionAzabicyclo[2.2.2 ]octan-5-oneSodium arene sulfonate α-ZrPAChE inhibition Aza-Diels-Alder cycloadditionAzabicyclo[2.2.2 ]octan-5-oneSodium calix[4]arene sulfonate α-ZrPAChE inhibition
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