Recent Advances in the Synthesis of Fused Heterocyclic Compounds and Their Antitumor Activities

被引:3
|
作者
Duan Kanghui [1 ]
Tang Junlong [1 ]
Wu Wanqing [1 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Key Lab Funct Mol Engn Guangdong Prov, Guangzhou 510690, Peoples R China
基金
中国国家自然科学基金;
关键词
unsaturated hydrocarbons; transition metal-catalysis; fused heterocyclic compounds; antitumor activity; BIOACTIVE BENZOFURAN DERIVATIVES; AZOMETHINE YLIDES; 3+3 ANNULATION; PALLADIUM; INDOLE; BENZOTHIAZOLE; CYCLIZATION; ACCESS; ANTICANCER; COPPER;
D O I
10.6023/cjoc202211046
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The unique physicochemical properties invest fused heterocyclic compounds with wide applications in the synthesis of natural products, drugs, superconducting materials, energy storage materials, polymer materials, organic dyes, etc. In recent years, the rapid development of transition metal-catalyzed reactions of unsaturated hydrocarbons has developed rapidly. Owing to the advantages of high step- and atom-economy, easy availability of raw starting materials, and efficient construction of carbon-carbon bonds or/and carbon-hetero bonds, it is a vital way to synthesize fused heterocyclic compounds. Herein, the recent progress on the reaction development of transition metal-catalyzed cyclizations involving unsaturated hydrocarbons for the synthesis of fused heterocyclic compounds including benzofurans, indoles, quinolines in the last five years has been summarized, as well as their applications in the field of medicinal chemistry with antitumor activities.
引用
收藏
页码:826 / 854
页数:29
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