Atroposelective Construction of Tetrasubstituted Axially Chiral Alkene Frameworks

被引:7
|
作者
Zou, Jia-Yu [1 ]
Xu, Wan-Yi [1 ]
Wang, Jie [1 ]
Liu, Qi [1 ]
He, Ying [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Chem & Chem Engn, Xiaolingwei 200, Nanjing 210094, Peoples R China
来源
SYNTHESIS-STUTTGART | 2024年 / 56卷 / 12期
基金
中国国家自然科学基金;
关键词
axial chirality; tetrasubstituted alkenes; difunctionalization; C-H functionalization; cross-coupling; kinetic resolution; asymmetric allylic substitution-isomerization; ASYMMETRIC OLEFIN ISOMERIZATION; ENANTIOSELECTIVE SYNTHESIS; ALLYLIC SUBSTITUTION; ATROPISOMERS; CATALYSIS; FUNCTIONALIZATION; ORGANOCATALYSIS; DEAROMATIZATION; STEREOCENTERS; STYRENES;
D O I
10.1055/a-2230-0759
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The construction of axially chiral alkene frameworks is currently one of hottest topics in the field of organic synthetic chemistry. Compared to traditional axially chiral molecules, such as biaryls, heterobiaryls, and anilides, the synthesis of axially chiral alkenes is far more challenging, especially for acyclic tetrasubstituted alkene analogues. In this review, we summarized the development of strategies for the synthesis of tetrasubstituted axially chiral alkene analogues, including asymmetric difunctionalization, C-H functionalization, cross-coupling, (dynamic) kinetic resolution, and asymmetric allylic substitution-isomerization. 1 Introduction 2 Synthesis of Cyclic Tetrasubstituted Axially Chiral Alkenes 3 Synthesis of Acyclic Tetrasubstituted Axially Chiral Alkenes 4 Summary and Outlook
引用
收藏
页码:1862 / 1872
页数:11
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