首页> 外文期刊>Russian Journal of Organic Chemistry >d]isoxazol-4(5 H)-ones and 6,7-Dihydro-1 H-indazol-4(5 H)-ones with Isoxazole and Isoxazoline Fragments in the Side Chain]]>
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d]isoxazol-4(5 H)-ones and 6,7-Dihydro-1 H-indazol-4(5 H)-ones with Isoxazole and Isoxazoline Fragments in the Side Chain]]>

机译:<![CDATA [5,5-二甲基-2-(3-芳基-4-硝酸丁酰基)环己烷-1,3-致的化学转化。 6,7-二氢苯并的合成[<重点型=“斜体”> D ]异恶唑-4(5 <重点型=“斜体”> H ) - α和6,7-二氢 - 1 <重点类型=“斜体”> H -indazol-4(5 <重点型=“斜体”> h ) - 侧链中的异恶唑和异恶唑啉碎片]]>

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摘要

By reaction of 5,5-dimethyl-2-(3-aryl-4-nitrobutanoyl)cyclohexane-1,3-diones with hydroxylamine and hydrazine hydrate 6,7-dihydrobenzo[d]isoxazol-4(5 H )-ones and 6,7-dihydro-1 H -indazol-4(5H)-ones were prepared containing a nitromethyl substituent in the side chain. Basing on the nitromethyl group of the latter nitrile oxide intermediates were generated that were brought into reaction of 1,3-dipolar addition with phenylacetylene, styrene, and vinyl ethyl ether with the formation of the corresponding isoxazole and isoxazoline derivatives.
机译:通过将5,5-二甲基-2-(3-芳基-4-硝酸丁酰基)环己烷-1,3-致反应与羟胺和肼水合物6,7-二氢苯并[d]异恶唑-4(5 h) - 在侧链中含有氮甲基取代基制备6,7-二氢-1 H-Indazol-4(5H)酮。 基于后一种腈氧化物中间体的硝基甲基,产生与苯乙烯,苯乙烯和乙烯基乙醚的1,3-偶极加入的反应,形成相应的异恶唑和异恶唑啉衍生物。

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    Institute of Bioorganic Chemistry of National Academy of Sciences of Belarus;

    Institute of Bioorganic Chemistry of National Academy of Sciences of Belarus;

    Institute of Bioorganic Chemistry of National Academy of Sciences of Belarus;

    Institute of Bioorganic Chemistry of National Academy of Sciences of Belarus;

    Institute of Bioorganic Chemistry of National Academy of Sciences of Belarus;

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  • 正文语种 eng
  • 中图分类 有机化学;
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