Oxy-Alkylation of Allylamines with Unactivated Alkyl Bromides and CO2 via Visible-Light-Driven Palladium Catalysis

被引:111
作者
Sun, Liang [1 ]
Ye, Jian-Heng [1 ]
Zhou, Wen-Jun [1 ,2 ]
Zeng, Xin [1 ]
Yu, Da-Gang [1 ]
机构
[1] Sichuan Univ, Coll Chem, Minist Educ, Key Lab Green Chem & Technol, Chengdu 610064, Sichuan, Peoples R China
[2] Neijiang Normal Univ, Coll Chem & Chem Engn, Neijiang 641112, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H BONDS; TRANSITION-METAL-FREE; HECK REACTION; COUPLING REACTIONS; RECENT PROGRESS; CARBON-DIOXIDE; DUAL CATALYSIS; ATOM-TRANSFER; CARBOXYLATION; PHOTOREDOX;
D O I
10.1021/acs.orglett.8b01079
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A selective oxy-alkylation of allylamines with unactivated alkyl bromides and CO2 via visible-light-driven palladium catalysis is reported. The commercially available Pd(PPh3)(4) is used as the sole catalyst in this three component reaction. A variety of tertiary, secondary, and primary alkyl bromides undergo reactions to generate important 2-oxazolidinones in high yields and selectivity. The mild reaction conditions, easy scalability, and facile derivatization of products provide great potential for application in organic synthesis and pharmaceutical chemistry.
引用
收藏
页码:3049 / 3052
页数:4
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