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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >FORMATION PATHWAY OF NOVEL CYCLOADDUCT OBTAINED BY REACTION OF 3,5-DISUBSTITUTED 4-OXO-4H-PYRAZOLE 1,2-DIOXIDE WITH DIMETHYL ACETYLENEDICARBOXYLATE
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FORMATION PATHWAY OF NOVEL CYCLOADDUCT OBTAINED BY REACTION OF 3,5-DISUBSTITUTED 4-OXO-4H-PYRAZOLE 1,2-DIOXIDE WITH DIMETHYL ACETYLENEDICARBOXYLATE

机译:3,5-二取代的4-OXO-4H-吡唑1,2-二氧化物与对乙酰二甲酸二甲酯的反应获得的新型循环载荷的形成途径

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摘要

A new formation pathway via [3,3]-sigmatropic rearrangement of the 1,3-dipolar reaction product was proposed for the novel nitrogen-free compound formed from the reaction of 3,5-disubstituted 4-oxo-4H-pyrazole 1,2-dioxide with dimethyl acetylenedicarboxylate.
机译:对于由3,5-二取代的4-oxo-4H-吡唑1反应形成的新型无氮化合物,提出了一种通过1,3-偶极反应产物的[3,3]-σ重排的新形成途径。 2-二氧化物与乙炔二甲酸二甲酯。

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