Highly Regio- and Enantioselective Synthesis of N-Substituted 2-Pyridones: Iridium-Catalyzed Intermolecular Asymmetric Allylic Amination
Zhang X(张霄); Yang ZP(杨泽鹏); Huang L(黄林); You SL(游书力)
刊名Angew. Chem.-Int. Edit.
2015
卷号54期号:6页码:1873-1876
其他题名金属铱催化的不对称烯丙基胺化反应高区域选择性和对映选择性合成N-取代2-吡啶酮
通讯作者游书力
英文摘要The first iridium-catalyzed intermolecular asymmetric allylic amination reaction with 2-hydroxypyridines has been developed, thus providing a highly efficient synthesis of enantioenriched N-substituted 2-pyridone derivatives from readily available starting materials. This protocol features a good tolerance of functional groups in both the allylic carbonates and 2-hydroxypyridines, thereby delivering multifunctionalized heterocyclic products with up to 98% yield and 99%ee.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/anie.201409976
语种英语
WOS记录号WOS:000349209200035
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/39564]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位中科院上海有机化学研究所, 金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
Zhang X,Yang ZP,Huang L,et al. Highly Regio- and Enantioselective Synthesis of N-Substituted 2-Pyridones: Iridium-Catalyzed Intermolecular Asymmetric Allylic Amination[J]. Angew. Chem.-Int. Edit.,2015,54(6):1873-1876.
APA 张霄,杨泽鹏,黄林,&游书力.(2015).Highly Regio- and Enantioselective Synthesis of N-Substituted 2-Pyridones: Iridium-Catalyzed Intermolecular Asymmetric Allylic Amination.Angew. Chem.-Int. Edit.,54(6),1873-1876.
MLA 张霄,et al."Highly Regio- and Enantioselective Synthesis of N-Substituted 2-Pyridones: Iridium-Catalyzed Intermolecular Asymmetric Allylic Amination".Angew. Chem.-Int. Edit. 54.6(2015):1873-1876.
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