中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective Synthesis of Pyrrole-Based Spiro- and Polycyclic Derivatives by Iridium-Catalyzed Asymmetric Allylic Dearomatization and Controllable Migration Reactions

文献类型:期刊论文

作者Zhuo CX(卓春祥); Cheng Q(程强); Liu WB(刘文博); Zhao Q(赵强); You SL(游书力)
刊名Angew. Chem.-Int. Edit.
出版日期2015
卷号54期号:29页码:8475-8479
其他题名通过铱催化的不对称烯丙基去芳构化和可控的迁移反应不对称合成螺环和多环吡咯衍生物
通讯作者游书力
英文摘要The first highly diastereo- and enantioselective synthesis of five-membered spiro-2H-pyrroles was achieved using an Ir-catalyzed asymmetric allylic dearomatization reaction. The spiro-2H-pyrrole derivatives readily undergo a controllable and stereospecific allylic migration under acid catalysis, providing polycyclic pyrrole derivatives in excellent yields and ee values. Additionally, the novel Ir-complex K1, derived from [Ir(cod) Cl](2) (cod= 1,5-cyclooctadiene) and N-benzhydryl-N-phenyldinaphthophosphoramidite (BHPphos), showed excellent control of both diastereo- and enantioselectivities.
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.201502259
语种英语
WOS记录号WOS:000358050300029
源URL[http://ir.sioc.ac.cn/handle/331003/39620]  
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
Zhuo CX,Cheng Q,Liu WB,et al. Enantioselective Synthesis of Pyrrole-Based Spiro- and Polycyclic Derivatives by Iridium-Catalyzed Asymmetric Allylic Dearomatization and Controllable Migration Reactions[J]. Angew. Chem.-Int. Edit.,2015,54(29):8475-8479.
APA 卓春祥,程强,刘文博,赵强,&游书力.(2015).Enantioselective Synthesis of Pyrrole-Based Spiro- and Polycyclic Derivatives by Iridium-Catalyzed Asymmetric Allylic Dearomatization and Controllable Migration Reactions.Angew. Chem.-Int. Edit.,54(29),8475-8479.
MLA 卓春祥,et al."Enantioselective Synthesis of Pyrrole-Based Spiro- and Polycyclic Derivatives by Iridium-Catalyzed Asymmetric Allylic Dearomatization and Controllable Migration Reactions".Angew. Chem.-Int. Edit. 54.29(2015):8475-8479.

入库方式: OAI收割

来源:上海有机化学研究所

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