Pd-catalyzed enantioselective [4+4] dipolar cycloaddition of aliphatic 1,4-dipoles with azadienes to access eight-membered N-heterocycles

被引:7
|
作者
Chen, Gen-Hui [1 ]
Ye, Ying [1 ]
Zhang, De-Xin [1 ]
Li, Hong-Jiao [1 ]
Zhang, Ning [1 ]
Liang, Guo-Juan [1 ]
Zhang, Dong [1 ]
Zhou, Jing [1 ]
Zhou, Hui [1 ]
机构
[1] Chongqing Med Univ, Coll Pharm, Chongqing Res Ctr Pharmaceut Engn, Chongqing 400016, Peoples R China
基金
中国国家自然科学基金;
关键词
REARRANGEMENT; CONSTRUCTION; IMINES;
D O I
10.1039/d3qo01089a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The construction of eight-membered N-heterocycles with good diastereo- and enantioselective control remains a formidable challenge in asymmetric catalysis. Herein, we report a palladium-catalyzed asymmetric [4 + 4] dipolar cycloaddition of aliphatic 1,4-dipoles with azadienes, furnishing chiral benzofuran- and indene-fused eight-membered N-heterocycles in good yields (up to 86%) and excellent stereoselectivities (up to >20 : 1 dr, 95% ee). This reaction not only represents the first catalytic asymmetric [4 + 4] cyclization of aliphatic 1,4-dipoles but also provides a new and efficient way to construct a variety of novel chiral fused eight-membered N-heterocycles.
引用
收藏
页码:4698 / 4702
页数:5
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