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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of Oxa-aza- and Bis-oxathiaaza[3.3.3]propellanes from Dicyanomethylene-1,3-indanedione and 2,5-Dithiobiureas
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Synthesis of Oxa-aza- and Bis-oxathiaaza[3.3.3]propellanes from Dicyanomethylene-1,3-indanedione and 2,5-Dithiobiureas

机译:由二氰基亚甲基-1,3-茚满二酮和2,5-二硫代双脲合成氧杂氮杂和双恶杂氮杂[3.3.3]丙炔酮

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摘要

An efficient route for the synthesis of oxa-aza-and bis-oxathiaaza[3.3.3]propellanes via reactions of symmetrical and unsymmetrical N-1,N-2-disubstituted hydrazine-1,2-dicarbothioamides (2,5-dithiobiureas) with (1,3-dioxo-2,3-dihydro-1H-inden-2-ylidene) propanedinitrile in tetrahydrofuran is described. The rationale behind these conversions involving nucleophilic addition on the dicyanomethylene carbon atom is presented. The structures of these unusual products are confirmed by X-ray crystal structure analysis.
机译:通过对称和不对称的N-1,N-2-二取代肼-1,2-二硫代硫代酰胺(2,5-dithiobiureas)反应合成oxa-氮杂和双-oxathiaaza [3.3.3]丙炔的有效途径描述了在四氢呋喃中由(1,3-二氧代-2,3-二氢-1H-茚满-2-亚烷基)丙烷化的丙炔。这些转化背后的原理涉及在二氰基亚甲基碳原子上的亲核加成。这些异常产物的结构通过X射线晶体结构分析确认。

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