Synthesis of α-chiral amides via synergistic visible-light-induced Wolff rearrangement and asymmetric NHC catalysis

被引:0
|
作者
Wang, Jiaomei [1 ]
Chen, Yangxu [2 ]
Miao, Siyan [2 ]
Yao, Changsheng [2 ]
Zhang, Kai [2 ]
机构
[1] Xuzhou Univ Technol, Sch Mat & Chem Engn, Xuzhou 221018, Peoples R China
[2] Jiangsu Normal Univ, Sch Chem & Mat Sci, Jiangsu Key Lab Green Synthet Chem Funct Mat, Xuzhou 221116, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
ENANTIOSELECTIVE BETA-PROTONATION; HETEROCYCLIC CARBENE CATALYSIS; SATURATED CARBOXYLIC-ACID; KETENES; AMINES; ESTERIFICATION; HYDROGENATION; DERIVATIVES; COUPLINGS; STRATEGY;
D O I
10.1039/d4nj03410d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, a visible-light-induced chiral N-heterocyclic carbene (NHC)-catalyzed asymmetric amination of ketenes has been developed. This strategy provides a convenient and facile synthetic protocol for the efficient construction of alpha-chiral amides under mild reaction conditions with moderate to excellent yields and stereoselectivities (up to 95% yields and 97 : 3 e.r.). Furthermore, a chiral 2-phenyl-1-propylamine derivative and (R)-ibuprofen could be obtained after simple transformations of the chiral products.
引用
收藏
页码:15287 / 15291
页数:5
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