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首页> 外文期刊>Tetrahedron >An efficient protocol for the synthesis of six-membered N, O-heterocycles via a 1,3-dipolar (3+3) cycloaddition between nitrile oxide and α-diazo esters
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An efficient protocol for the synthesis of six-membered N, O-heterocycles via a 1,3-dipolar (3+3) cycloaddition between nitrile oxide and α-diazo esters

机译:一种有效的合成六元N,O-杂环通过 1,3-偶极(3 + 3)环加成腈氧化物和α< / ce:斜体> -diazo酯

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摘要

Abstract In this manuscript, we are reporting an efficient protocol for the construction of highly functionalized N, O-heterocyclic derivatives such as 1,2,4-oxadiazine and 1,4,2-dioxazine-6-carboxylate derivatives via a 1,3-dipolar (3?+?3) cycloaddition between nitrile oxide and unprotected α-diazo esters in the presence of 2?mol% Cu(OTf)2 catalyst. The expected N, O-heterocycles were obtained in excellent yields. These N, O-heterocycles are known to exhibit insecticidal and acaricidal properties. Graphical abstract Display Omitted Highlights ? This is a convenient protocol for the con
机译:<![CDATA [ 抽象 在本手稿中,我们报告了一种高效的协议,用于构建高官能化N,O-杂环衍生物作为1,2,4-氧代嗪和1,4,2-二恶嗪-6-羧酸盐衍生物通过 1,3-偶极(3→+ 3)环加成腈氧化物并且无保护α -diazo酯在2?mol%cu(otf) 2 催化剂。预期的N,O-杂环以优异的产率获得。已知这些N,O-杂拷贝表现出杀虫和杀螨特性。 图形摘要 显示省略 突出显示 这是一个方便的协议con

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