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作 者:WANG Hui NIU Xiao-di ZHAO Min XIAO Xue-bin WANG Hong-su WANG Zhong-dong
机构地区:[1]Teaching Center of Basic Courses, Jilin University, Changchun 130062, P. R. China, [2]Department of Chemistry, Mudanjiang Teachers College, Mudanjiang 157012, P. R. China
出 处:《Chemical Research in Chinese Universities》2011年第4期664-668,共5页高等学校化学研究(英文版)
基 金:Supported by the Research Startup Fund of Jilin University,China(Nos.4305050102H8,4305050102B5);the Basic Research and Operational Costs of Jilin University,China(Nos.421031196604,450060445293)
摘 要:Benzyl and anthracenemethyl groups were respectively bonded to the N atoms of 3-aminopropyl functionalized mesoporous SBA-15(APS-SBA-15) to obtain two new base catalysts over which the condensation reaction of benzaldehyde and 2'-hydroxyacetophenone was studied.Good catalytic activities and high selectivities for flavanones were obtained in solvent-free reactions,which is attributed to the effect of benzyl and anthracenemetyl groups on the base sites of catalysts and the steric hindrance of futher reaction of flavanone with benzaldehyde.Benzyl and anthracenemethyl groups were respectively bonded to the N atoms of 3-aminopropyl functionalized mesoporous SBA-15(APS-SBA-15) to obtain two new base catalysts over which the condensation reaction of benzaldehyde and 2'-hydroxyacetophenone was studied.Good catalytic activities and high selectivities for flavanones were obtained in solvent-free reactions,which is attributed to the effect of benzyl and anthracenemetyl groups on the base sites of catalysts and the steric hindrance of futher reaction of flavanone with benzaldehyde.
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