Transition metal-free synthesis of α-aryl ketones via oxyallyl cation capture with arylboronic acids

被引:12
|
作者
Huang, Wei-Hua [1 ]
Huang, Gong-Bin [1 ]
Zhu, Wen-Run [1 ]
Weng, Jiang [1 ]
Lu, Gui [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Design & Evaluat, Guangzhou 510006, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2020年 / 7卷 / 17期
基金
中国国家自然科学基金;
关键词
4+3 CYCLOADDITION REACTION; CROSS-COUPLINGS; BORONIC ACIDS; ARYLATION; INTERMEDIATE; CARBON; FUNCTIONALIZATION; ACTIVATION; REACTIVITY; FLUORINE;
D O I
10.1039/d0qo00447b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, we describe a novel transition metal-free, umpolung strategy for the alpha-arylation of ketones by capturing transient oxyallyl cations with arylboronic acids. A variety of alpha-arylated ketones were obtained in moderate to good yields with broad substrate tolerance under simple reaction conditions. This process provides a complementary strategy compared with traditional transition metal-catalyzed methods.
引用
收藏
页码:2480 / 2485
页数:6
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