Progress in the catalytic enantioselective construction of difluoroalkylated stereogenic centers

被引:0
|
作者
Tang, Li-Juan [1 ]
Wen, Yongshun [1 ]
Jin, Hong-Xian [1 ]
Luo, Wenjun [1 ]
Long, Lipeng [1 ]
Shen, Jiayi [1 ]
Luo, Haiqing [1 ]
Yu, Daohong [1 ]
机构
[1] Gannan Normal Univ, Optoelect Funct Mat Ctr, Jiangxi Prov Key Lab Synthet Pharmaceut Chem, Ganzhou 341000, Jiangxi, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2025年 / 12卷 / 06期
基金
中国国家自然科学基金;
关键词
ASYMMETRIC FLUORINATION; REFORMATSKY REACTION; ALLYLIC ALKYLATION; BETA-KETOESTERS; ALDOL REACTIONS; CARBON CENTERS; TRIFLUOROMETHYLATION; ALPHA; ESTERS; ACID;
D O I
10.1039/d4qo02309a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Molecules bearing difluoroalkyl groups are very important in pharmaceuticals, agrochemicals, and many materials. In recent years, significant attention has been paid to the development of novel synthetic methods for constructing compounds containing CF2R groups. In particular, the construction of difluoroalkylated stereogenic centers is thriving. This review focuses on catalytic asymmetric difluoroalkylation for the construction of difluoralkylated stereogenic centers, summarizing the reported synthetic methods, the active intermediates involved, and the asymmetric strategies applied. The product diversity, selectivity, and proposed mechanisms are highlighted, and the future outlook and existing challenges are also provided.
引用
收藏
页码:2052 / 2075
页数:24
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