NHC catalyzed radical tandem cyclization: an efficient synthesis of α,α-difluoro-γ-lactam derivatives

被引:0
|
作者
Huang, Tianjiao [1 ]
Yin, Huiping [1 ]
Li, Tuanjie [1 ]
Yu, Chenxia [1 ]
Zhang, Kai [1 ]
Yao, Changsheng [1 ]
机构
[1] 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
AMINODIFLUOROALKYLATION; LACTAMS; ACID;
D O I
10.1039/d4ob01012d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, an N-heterocyclic carbene (NHC) catalyzed radical tandem cyclization reaction of N-allylbromodifluoroacetamides and aldehydes has been developed. This method is an efficient protocol for synthesizing alpha,alpha-difluoro-gamma-lactam derivatives in moderate to good yields (27 examples, up to 88% yield and 10 : 1 dr). This strategy features mild and metal-free conditions, high efficiency, and a broad substrate scope. An N-heterocyclic carbene catalyzed radical tandem cyclization reaction of N-allylbromodifluoroacetamides and aldehydes has been developed. This method provides a protocol for synthesizing alpha,alpha-difluoro-gamma-lactam derivatives in moderate to good results (27 examples, up to 88% yield, 10 : 1 d.r.).
引用
收藏
页码:6988 / 6998
页数:11
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