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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
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2017-09-08 , DOI: 10.1016/j.tetlet.2017.09.015
Alexey Y. Barkov , Nikolay S. Zimnitskiy , Igor B. Kutyashev , Vladislav Y. Korotaev , Vyacheslav Y. Sosnovskikh

The reactions of 3-nitro-2-phenyl-2H-chromenes with 2-arylmethylidene-5-oxopyrazolidin-2-ium-1-ides proceeded diastereoselectively to afford the corresponding tetrahydrochromeno[4,3-c]pyrazolo[1,2-a]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 Δ3-bond of the chromene system.



中文翻译:

稳定的NN'-环偶氮甲亚胺与3-硝基-2-苯基-2 H-色烯的高度立体选择性[3 + 2] -环加成反应:合成四氢色素[4,3- c ]吡唑并[1,2-一个]吡唑-11-那些

3-硝基-2-苯基-2 H-色烯与2-芳基亚甲基-5-氧吡唑并丁-2-鎓-1的反应非对映选择性地进行,得到相应的四氢色素[4,3- c ]吡唑并[1,2]。 -一个]吡唑11酮以良好的收率作为稳定1,3-偶极环加成反应的结果ññ在Δ' -环甲亚胺亚胺3色烯系统的-键。

更新日期:2017-09-08
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