DABCO-catalyzed [3+2] cycloaddition reactions of azomethine imines with N-aryl maleimides: facile access to dinitrogen-fused heterocycles

被引：23
|
作者：
Jia, Qianfa [1 ]
Chen, Lei [1 ]
Yang, Gongming [1 ]
Wang, Jian [1 ]
Wei, Jia [1 ]
Du, Zhiyun [1 ]
机构：
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Inst Nat Med & Green Chem, Allan H Conney Lab Anticanc Res, Guangzhou 510006, Guangdong, Peoples R China
来源：
TETRAHEDRON LETTERS | 2015年 / 56卷 / 52期
基金：
中国国家自然科学基金;
关键词：
3+2] cycloaddition; N; C-Azomethine imine; Maleimide; DABCO catalysis; DIPEPTIDYL-PEPTIDASE-IV; IMPROVED GLUCOSE-TOLERANCE; 1,3-DIPOLAR CYCLOADDITIONS; DERIVATIVES; INHIBITOR; ALLENOATES; ALDEHYDES; RATS;
D O I：
10.1016/j.tetlet.2015.11.030
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
DABCO-catalyzed [3+2] cycloaddition of azomethine imines with maleimides has been developed. This method could efficiently furnish dinitrogen-fused tetracyclic heterocycles in high levels of regioselectivity and with good yields. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码：7150 / 7153
页数：4
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