Recent advances in the synthesis of nitrogen heterocycles via radical cascade reactions using isonitriles as radical acceptors

被引:699
|
作者
Zhang, Bo [1 ]
Studer, Armido [2 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[2] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
关键词
FLUOROUS-TAGGING STRATEGY; OXIDATIVE CYCLIZATION; METAL-FREE; ARYL ISONITRILES; PHENANTHRIDINE DERIVATIVES; EFFICIENT SYNTHESIS; ARYLBORONIC ACIDS; MAPPICINE ANALOGS; VINYL ISOCYANIDES; 2-ISOCYANOBIPHENYLS;
D O I
10.1039/c5cs00083a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nitrogen heterocycles belong to a highly important class of compounds which are found in various natural products, biologically active structures, and medicinally relevant compounds. Therefore, there is continuing interest in the development of novel synthetic methods for the construction of nitrogen containing heterocycles. Recently, radical insertion reactions into isonitriles have emerged as an efficient and powerful strategy for the construction of nitrogen heterocycles, such as phenanthridines, indoles, quinolines, quinoxalines, and isoquinolines. This review highlights recent advances in this fast growing research area and also includes important pioneering studies in this area.
引用
收藏
页码:3505 / 3521
页数:17
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