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作 者:毛璞[1] 朱军亮 袁金伟[1] 杨亮茹[1] 肖咏梅[1] 张长森[2] Mao Pu;Zhu Junliang;Yuan Jinwei;Yang Liangru;Xiao Yongmei;Zhang Changsen(Academician Workstation for Natural Medicinal Chemistry of Henan Province,School of Chemistry & Chemical Engineering,Henan Univeristy of Technology,Zhengzhou 450001;College of Chemistry and Molecular Engineering,Zhengzhou University,Zhengzhou 450001)
机构地区:[1]河南工业大学化学化工学院河南省天然药物化学院士工作站,郑州450001 [2]郑州大学化学与分子工程学院,郑州450001
出 处:《有机化学》2019年第6期1529-1547,共19页Chinese Journal of Organic Chemistry
基 金:Project supported by the Department of Henan Province Natural Science and Technology Foundation(Nos.172102210225 and 182102310675);the Natural Science Foundation in Henan Province Department of Education(No.17A150005);the Program for Innovative Research Team from Zhengzhou(No.131PCXTD605);the Project of Youth Backbone Teachers of Henan University of Technology(No.2016003)~~
摘 要:喹喔啉-2(1H)-酮是天然产物和药物中存在的一种非常重要的N-杂环化合物,具有广泛的生物活性.近年来,研究者对喹喔啉-2(1H)-酮的C-H键活化和功能化的进行了大量的研究,包括烷基化、苄基化、酰化、芳基化、胺化、酰胺化、膦酰化、氟烷基化等.综述了近年来该领域的研究进展,并对其反应机理进行了探讨.Quinoxalin-2(1H)-ones are very important N-heterocyclic moieties found in natural products and pharmaceuticals,and exhibit an amazingly wide spectrum of biological properties.Numerous efforts have been devoted to the development of efficient approaches for the C-H bond activation and functionalization of quinoxalin-2(1H)-ones in recent years,including alkylation,benzylation,acylation,arylation,amination,amidation,phosphonation,and fluoroalkylation.The recent advances in this area are summarized and their reaction mechanisms are discussed.
关 键 词:喹喔啉-2(1H)-酮 C-H键活化 功能化 过渡金属催化
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