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首页> 外文期刊>Molecular diversity >Synthesis of functionalized 5-imino-2,5-dihydro-furans through the reaction of isocyanides with activated acetylenes in the presence of ethyl bromopyruvate
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Synthesis of functionalized 5-imino-2,5-dihydro-furans through the reaction of isocyanides with activated acetylenes in the presence of ethyl bromopyruvate

机译:在溴代丙酮酸乙酯存在下,异氰酸酯与活化的乙炔反应,合成官能化的5-亚氨基-2,5-二氢呋喃

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摘要

The reaction between alkyl(aryl) isocyanides and dibenzoylacetylene in the presence of ethyl bromopyruvate leads to ethyl 3,4-dibenzoyl-2-bromomethyl-5-alkyl(aryl)imino-2,5-dihydro-furan-2-carboxylates in high yields. Dialkyl acetylenedicarboxylates react with tert-butyl isocyanide and ethyl bromopyruvate to produce 3,4-dialkyl 2-ethyl 2-bromomethyl-5-tert-butylimino-2,5dihydro-furan-2,3,4-tricarboxylates.
机译:在溴丙酮酸乙酯存在下,烷基(芳基)异氰酸酯与二苯甲酰基乙炔之间的反应可在高浓度下生成3,4-二苯甲酰基-2-溴甲基-5-烷基(芳基)亚氨基-2,5-二氢呋喃-2-羧酸乙酯产量。乙炔二羧酸二烷基酯与异氰酸叔丁基酯和溴丙酮酸乙酯反应生成3,4-二烷基-2-乙基-2-溴甲基-5-叔丁基亚氨基-2,5-二氢呋喃-2,3,4-三羧酸酯。

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