中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Iridium-Catalyzed Allylic Vinylation and Asymmetric Allylic Amination Reactions with o-Aminostyrenes

文献类型:期刊论文

作者Ye KY(叶克印) ; He H(贺虎) ; Liu WB(刘文博) ; Dai LX(戴立信) ; HELMCHEN GUENTER ; You SL(游书力)
刊名J. Am. Chem. Soc.
出版日期2011
卷号133期号:46页码:19006-19014
ISSN号0002-7863
其他题名铱催化的邻氨基苯乙烯的烯丙基烯基化和不对称烯丙基胺化反应
通讯作者游书力
英文摘要An Ir-catalyzed allylic vinylation reaction of allyl carbonates with o-aminostyrene derivatives has been realized, providing skipped (Z,E)-diene derivatives. With (E)-but-2-ene-1,4-diyl dimethyl dicarbonate as the substrate, an efficient enantioselective synthesis of 1-benzazepine derivatives via an Ir-catalyzed domino allylic vinylation/intramolecular allylic amination reaction has been developed. Mechanistic studies of the allylic vinylation reaction have been carried out, and the results suggest that the leaving group of the allylic precursor plays a key role in directing the reaction pathway. Screening of various allylic precursors showed that Ir-catalyzed reactions of allyl diethyl phosphates with o-aminostyrene derivatives proceed via an allylic animation pathway. A subsequent ring-closing metathesis (RCM) reaction of the amination products led to a series of enantiomerically enriched 1,2-dihydroquinoline derivatives. Their utility is indicated by an asymmetric total synthesis of (-)-angustureine.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ja2092954
语种英语
WOS记录号WOS:000297398900072
公开日期2013-02-19
源URL[http://202.127.28.38/handle/331003/16021]  
专题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
Ye KY,He H,Liu WB,et al. Iridium-Catalyzed Allylic Vinylation and Asymmetric Allylic Amination Reactions with o-Aminostyrenes[J]. J. Am. Chem. Soc.,2011,133(46):19006-19014.
APA 叶克印,贺虎,刘文博,戴立信,HELMCHEN GUENTER,&游书力.(2011).Iridium-Catalyzed Allylic Vinylation and Asymmetric Allylic Amination Reactions with o-Aminostyrenes.J. Am. Chem. Soc.,133(46),19006-19014.
MLA 叶克印,et al."Iridium-Catalyzed Allylic Vinylation and Asymmetric Allylic Amination Reactions with o-Aminostyrenes".J. Am. Chem. Soc. 133.46(2011):19006-19014.

入库方式: OAI收割

来源:上海有机化学研究所

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