首页> 外文期刊>Helvetica Chimica Acta >On the Reactions of Furan-2,3-diones with Oxindole (=1,3-Dihydro-2H-indol-2-one) and Lawesson Reagent. Synthesis of New 1,3-Dihydro-2H-indol-2-ones, Bis-furanones, and Bis-pyrrolones
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On the Reactions of Furan-2,3-diones with Oxindole (=1,3-Dihydro-2H-indol-2-one) and Lawesson Reagent. Synthesis of New 1,3-Dihydro-2H-indol-2-ones, Bis-furanones, and Bis-pyrrolones

机译:关于呋喃-2,3-二酮与羟吲哚(= 1,3-二氢-2H-吲哚-2-酮)和Lawesson试剂的反应。新型1,3-二氢-2H-吲哚-2-酮,双呋喃酮和双吡咯烷酮的合成

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摘要

Lactone analogues of 3-substituted oxindoles (=1,3-dihydro-2H-indol-2-ones) and nonbenzoid oxa-analogous isoindigoid or nonbenzoid isoindigoid dyes were prepared by the reactions of furan-2,3-diones with oxindole and Lawesson reagent (Schemes 1 and 3), respectively. So, new derivatives of 2-oxobutanoic acid, bis-furanone, and bis-pyrrolone, which are potentially biologically active compounds, were synthesized for the first time.
机译:通过呋喃-2,3-二酮与羟吲哚和Lawesson反应制备3-取代的羟吲哚的内酯类似物(= 1,3-二氢-2H-吲哚-2-酮)和非苯甲酰氧-类似异靛类或非苯甲酰异靛类染料。试剂(方案1和3)。因此,首次合成了具有潜在生物活性的2-氧代丁酸,双呋喃酮和双吡咯烷酮的新衍生物。

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