Radical Esterification of Unactivated Alkenes Using Formate asCarbonyl Source

被引:7
作者
Mu, Bing [1 ,2 ,3 ,4 ]
Xia, Shiwei [5 ]
Wu, Linna [5 ]
Li, Jingya [6 ]
Li, Zhongxian [7 ]
Wang, Zechao [5 ]
Wu, Junliang [1 ,2 ]
机构
[1] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Inst Green Catalysis, Zhengzhou 450001, Peoples R China
[3] Huzhou Univ, Coll Life Sci, Huzhou 313000, Zhejiang, Peoples R China
[4] Zhengzhou Normal Univ, Coll Chem & Chem Engn, Zhengzhou 450044, Peoples R China
[5] Zhengzhou Univ, Henan Inst Adv Technol, Div Mol Catalysis & Synth, Zhengzhou 450001, Peoples R China
[6] Leadmedpharm Co Ltd, Huzhou 313100, Zhejiang, Peoples R China
[7] Henan Acad Sci, High & New Technol Res Ctr, Zhengzhou 450002, Peoples R China
基金
中国国家自然科学基金;
关键词
PALLADIUM-CATALYZED CARBONYLATION; METHYL FORMATE; ARYL OLEFINS; FORMIC-ACID; HYDROESTERIFICATION; DIHYDROISOQUINOLINONES; ALKOXYCARBONYLATION; DERIVATIVES; EFFICIENT; ALKYNES;
D O I
10.1021/acs.joc.1c02808
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In recent years, methyl formate has receivedconsiderable attention as an ideal and green C1 building blockto synthesize carboxylic esters. However, examples of a one-steproute to esters with one-carbon elongation using methyl formate asa source of methoxycarbonyl radical are still rare. Herein, wepresent peroxide-induced radical carbonylation ofN-(2-methylallyl)benzamides with methyl formate as the precursor ofmethoxycarbonyl radical and RuCl3as catalyst, affording a series ofbiologically valuable 4-[(methoxycarbonyl)methyl]-3,4-dihydroiso-quinolinones with good tolerance and insensitivity to moisture inone pot under simple and mild conditions.
引用
收藏
页码:4918 / 4925
页数:8
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