Pd-Catalyzed Diastereo- and Enantioselective [3+2]-Cycloaddition Reaction of Vinyl Epoxide with Nitroalkenes

被引:43
|
作者
Wu, Wen-Qiong [1 ]
Ding, Chang-Hua [2 ]
Hou, Xue-Long [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Shanghai Hong Kong Joint Lab Chem Synth, Shanghai 200032, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
vinyl epoxide; nitroalkene; palladium; asymmetric catalysis; 3+2] cycloaddition; ASYMMETRIC CYCLOADDITION REACTIONS; SATURATED OXYGEN HETEROCYCLES; ACTIVATED OLEFINS; HECK REACTION; CASCADE REACTIONS; LIGANDS; TETRAHYDROFURANS; VINYLAZIRIDINES; CYCLOPROPANES; DERIVATIVES;
D O I
10.1055/s-0031-1290525
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A diastereoselective and enantioselective [3+2]-cycloaddition reaction of vinyl epoxide and nitroalkenes has been developed using Pd/1,1'-ferrocene-P, N-ligand, providing substituted tetrahydrofurans in high yields and with high diastereo- and enantioselectivities.
引用
收藏
页码:1035 / 1038
页数:4
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