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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Facile synthesis of tricyclic isoxazole-fused benzo[b]thiophene 1,1-dioxide derivatives via 1,3-dipolar cycloaddition
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Facile synthesis of tricyclic isoxazole-fused benzo[b]thiophene 1,1-dioxide derivatives via 1,3-dipolar cycloaddition

机译:通过1,3-偶极环加入的体内三环异恶唑熔融苯并[B]噻吩1,1-二氧化衍生物的合成

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摘要

A facile and efficient [3 + 2] 1,3-dipolar cycloaddition reaction of nitrile oxides generated in situ from hydroximoyl chlorides with benzo[b]thiophene 1,1-dioxides has been achieved for rapid access to tricyclic isoxazole-fused benzo[b]thiophene 1,1-dioxide derivatives in excellent yields (up to 98%) with high diastereoselectivities (dr > 19:1). The present process is characterized by mild reaction conditions and broad substrate scope. The conversion of the cycloadduct to other useful structure has also been achieved. The chemical structures of the typical compounds were confirmed by X-ray single-crystal structure analysis. (C) 2020 Published by Elsevier Ltd.
机译:已经实现了用苯并[b]噻吩1,1-二氧化噻吩苯甲酰氯原位原位产生的腈氧化物的腈氧化物的容易和有效的[3 + 2] 1,3-偶极环加入反应。快速进入三环异恶唑融合苯并[b ]噻吩1,1-二氧化氧化物衍生物,优异的产率(高达98%),具有高抗对抗性(Dr> 19:1)。 本方法的特征在于温和的反应条件和宽底物范围。 还实现了循环化对其他有用结构的转换。 通过X射线单晶结构分析证实了典型化合物的化学结构。 (c)2020由elestvier有限公司发布

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