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Baeyer-Villiger Oxidation of Cyclic Ketones Catalyzed by Amino Acid Ionic Liquids

周期的酉同类的 Baeyer-Villiger 氧化由氨基酸爱奥尼亚的液体催化

作     者:YU Fengli CHI Yujie GAO Chong CHEN Ruirui XIE Congxia YU Shitao YU Fengli;CHI Yujie;GAO Chong;CHEN Ruirui;XIE Congxia;YU Shitao

作者机构:State Key Laboratory Base of Eco-chemical EngineehngCollege of Chemistry and Molecular EngineeringQingdao University of Science and TechnologyQingdao 266042P.R.China College of Chemical EngineeringQingdao University of Science and TechnologyQingdao 266042P.R.China 

出 版 物:《Chemical Research in Chinese Universities》 (高等学校化学研究(英文版))

年 卷 期:2020年第36卷第5期

页      面:865-869页

核心收录:

学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学] 

基  金:Supported by the National Natural Science Foundation of China(No.21878166) the Taishan Scholar Project of Shandong Province,China(No.ts201511033) the Emphasis Development Plan of Shandong Province,China(Nos.2017GGX70102,2017GGX40107) the Open Project of the Chemistry Department in Qingdao University of Science and Technology of China(No.QUSTHX201811) 

主  题:Amino acid ionic liquid Baeyer-Villiger oxidation Cyclic ketone Lactone 

摘      要:A series of amino-acid-based ionic liquids was synthesized via one-step protonation of the corresponding L-amiiio acid by utilizing an array of proton *** catalytic activity of the amino-acid-based ionic liquids for the Baeyer-Villiger oxidation of cyclic ketones was investigated using cyclopentanone as a model ***-based ionic liquid[ProH]CF3SO3 was shown to exliibit thebest catalytic *** reaction condition was optimized to give the following reagent ratio of h(cyclopentanone):n(catalyst):w(H2O2)=1:0.06:4,60℃and 6 *** the optimum conditions,the conversion of cyclopentanone was 96.57%and the selectivity forδ-valerolactone was 73.01%.The catalytic activity was shown to be constant after 4 cycles.A simple treatment was allowed for the recover and the reuse of[ProH]*** successful utilization of[ProH]CF3SO3 to catalyze a host of cyclic ketones via Baeyer-Villiger oxidation clearly demonstrated the capacity of[ProH]CF3S03 to tolerate variation in the substrate.

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