Transition-metal-catalyst-free synthesis of anthranilic acid derivatives by transfer hydrogenative coupling of 2-nitroaryl methanols with alcohols/amines

被引:7
|
作者
Zhang, Shudi [1 ,2 ]
Tan, Zhenda [1 ,2 ]
Xiong, Biao [3 ]
Jiang, Huan Feng [1 ,2 ]
Zhang, Min [1 ,2 ,4 ]
机构
[1] South China Univ Technol, State Key Lab Pulp & Paper Engn, Sch Chem & Chem Engn, Guangzhou 510641, Guangdong, Peoples R China
[2] South China Univ Technol, Key Lab Funct Mol Engn Guangdong Prov, Sch Chem & Chem Engn, Guangzhou 510641, Guangdong, Peoples R China
[3] Nantong Univ, Sch Pharm, 19 Qixiu Rd, Nantong 226001, Jiangsu, Peoples R China
[4] Wuyi Univ, Sch Chem & Environm Engn, Jiangmen 529090, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
SELECTIVE TRANSFER HYDROGENATION; HOFMANN-TYPE REARRANGEMENT; NITROGEN BI-HETEROARENES; MONO-N-METHYLATION; FUNCTIONALIZED ANILINES; ALKYLATION; STRATEGY; ACCESS; AMINATION; IMIDES;
D O I
10.1039/c7ob02919e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
By using a transfer hydrogenative coupling strategy, we herein describe a new method for the efficient synthesis of anthranilic acid derivatives, a significantly important class of compounds with extensive applications in organic synthesis and the discovery of bioactive molecules, from 2-nitroaryl methanols and readily available alcohols/amines. The synthesis proceeds with the merits of no need for a transition metal catalyst, operational simplicity, broad substrate scope, good functional tolerance, and high step efficiency, which offers a useful alternative to access anthranilic acid derivatives.
引用
收藏
页码:531 / 535
页数:5
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