Highly stereoselective [3+2]-cycloaddition reaction of stabilised N,N′-cyclic azomethine imines with 3-nitro-2-phenyl-2H-chromenes: Synthesis of tetrahydrochromeno[4,3-c]pyrazolo[1,2-a]pyrazol-11-ones

被引:12
作者
Barkov, Alexey Y. [1 ]
Zimnitskiy, Nikolay S. [1 ]
Kutyashev, Igor B. [1 ]
Korotaev, Vladislav Y. [1 ]
Sosnovskikh, Vyacheslav Y. [1 ]
机构
[1] Ural Fed Univ, Inst Nat Sci & Math, Ekaterinburg 620000, Russia
关键词
3-Nitro-2-phenyl-2H-chromenes; 2-Arylmethylidene-5-oxopyrazolidin-2-ium-1-ides; 1,3-Dipolar cycloaddition; Tetrahydrochromeno[4,3-clpyrazolo[1,2-a]pyrazol-11-ones; 1,3-DIPOLAR CYCLOADDITION; ANTIBACTERIAL AGENTS; DERIVATIVES; YLIDES; PYRAZOLIDINONES; CHROMENES; CHEMISTRY; ACCESS;
D O I
10.1016/j.tetlet.2017.09.015
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reactions of 3-nitro-2-phenyl-2H-chromenes with 2-arylmethylidene-5-oxopyrazolidin-2-ium-1ides proceeded diastereoselectively to afford the corresponding tetrahydrochromeno[4,3-c]pyrazolo [1,2-c]pyrazol-11-ones in good yields as a result of the 1,3-dipolar cycloaddition reaction of stabilised N,N'-cyclic azomethine imines at the.6,3-bond of the chromene system. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3989 / 3992
页数:4
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