中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Catalytic asymmetric enamine protonation reaction

文献类型:期刊论文

作者Fu, Niankai; Zhang, Long; Luo, Sanzhong
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
出版日期JAN 28 2018
卷号16期号:4页码:510-520
英文摘要Enantioselective protonation, delivery of a proton to a carbanion intermediate, is the most straightforward and fundamental method for the preparation of a chiral tertiary carbon stereocenter. Recent efforts for this objective have been realized through enamine catalysis, which has now become a prominent catalytic strategy enabling a range of fascinating chiral transformations. This review will summarize recent advances in the field of enantioselective enamine protonation for the synthesis of optically active carbonyl compounds. Dynamic kinetic resolutions of alpha-substituted carbonyl compounds through enamine intermediates will be discussed as well.
WOS记录号WOS:000423400700001
源URL[http://ir.iccas.ac.cn/handle/121111/38820]  
专题化学研究所_其它
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GB/T 7714
Fu, Niankai,Zhang, Long,Luo, Sanzhong. Catalytic asymmetric enamine protonation reaction[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,JAN ,16(4):510-520.
APA Fu, Niankai,Zhang, Long,&Luo, Sanzhong.(JAN ).Catalytic asymmetric enamine protonation reaction.ORGANIC & BIOMOLECULAR CHEMISTRY,16(4),510-520.
MLA Fu, Niankai,et al."Catalytic asymmetric enamine protonation reaction".ORGANIC & BIOMOLECULAR CHEMISTRY 16.4(JAN ):510-520.

入库方式: OAI收割

来源:化学研究所

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