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作 者:Shanghui Tian Tian Luo Yanping Zhu Jie-Ping Wan
机构地区:[1]College of Chemistry and Chemical Engineering,Jiangxi Normal University,Nanchang 330022,China [2]School of Pharmacy,Key Laboratory of Molecular Pharmacology and Drug Evaluation,Ministry of Education,Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong,Yantai University,Yantai 264005,China
出 处:《Chinese Chemical Letters》2020年第12期3073-3082,共10页中国化学快报(英文版)
基 金:National Natural Science Foundation of China(Nos.21861019 and 21702091)for financial support。
摘 要:Chromone and flavone are both central backbones of natural products and clinical medicines.Synthesis of diversely functionalized chromones and flavones constitutes significant research contents of the modern synthetic science because abundant molecular libraries of such types are crucial in providing candidate compounds for the discovery of new pharmaceuticals and functional materials.The direct C—H bond activation or functionalization on these heterocyclic backbones provides highly powerful tools for the rapid accesses to densely functionalized chromone and flavone derivatives.Considering the importance of the functionalized chromone and flavone compounds as well as the notable advances in the synthesis of such products by direct C—H activation or functionalization,we review herein the research advances in the C—H bond activation and functionalization reactions of chro mone and flavones,in hope of showing the current states and promise of the research domain.
关 键 词:CHROMONES Flavones C—H bond ACTIVATION FUNCTIONALIZATION
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