Copper-catalyzed [3+2] annulation of O-acyl ketoximes with 2-aryl malonates for the synthesis of 3-aryl-4-pyrrolin-2-ones

被引:4
|
作者
Song, Xiao-Qing [1 ]
Qiang, Xiao-Qi [1 ]
Hu, Zi-Jun [1 ]
Lyu, Xinyu [1 ]
Tan, Sheng [1 ]
Yao, Changsheng [2 ]
Sun, Yong-Qiang [3 ]
Miao, Chun-Bao [1 ]
Yang, Hai-Tao [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Jiangsu Prov Key Lab Fine Petrochem Engn, Changzhou 213164, 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
[3] Changzhou Siyao Pharmaceut Co Ltd, Changzhou 213018, Peoples R China
关键词
ALPHA-CONVERTING-ENZYME; C-H ACTIVATION; INTERNAL OXIDANT; OXIME ACETATES; BOND; FUNCTIONALIZATION; CYCLIZATION; INHIBITORS; INDOLES; OLEFINS;
D O I
10.1039/d3cc00367a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A copper-catalyzed [3+2] annulation of O-acyl ketoximes with 2-aryl malonates for the concise synthesis of 3-aryl-4-pyrrolin-2-ones has been developed. The advantage of this method lies in the use of O-acyl oximes as an internal oxidant to generate the nucleophilic enamines and electrophilic p-quinone methides concurrently. The subsequent nucleophilic addition undergoes selectively on the a-C of malonates.
引用
收藏
页码:5225 / 5228
页数:4
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