对映选择合成
分子内力
杂原子
化学
催化作用
二茂铁
过渡金属
组合化学
选择性
立体化学
有机化学
戒指(化学)
电化学
物理化学
电极
作者
Dao‐Yong Zhu,Ping Chen,Ji‐Bao Xia
出处
期刊:Chemcatchem
[Wiley]
日期:2015-10-28
卷期号:8 (1): 68-73
被引量:125
标识
DOI:10.1002/cctc.201500895
摘要
Abstract This minireview focuses on recent advancements in the synthesis of planar chiral ferrocenes by means of transition‐metal‐catalyzed enantioselective C−H activation. Enantioenriched planar chiral ferrocenes are synthesized through simple straightforward asymmetric carbon−carbon or carbon−heteroatom bond‐formation reactions. In these reports, site selectivity of ferrocene C−H activation is controlled by two strategies, coordination direction and intramolecular cyclization. Herein the significance of these results is summarized.
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