首页> 外文期刊>Monatshefte für Chemie / Chemical Monthly >Synthesis of fully substituted iminolactones via a three-component condensation of isocyanides and acetylenic esters with 2-bromo-1-(4-bromophenyl)ethanone
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Synthesis of fully substituted iminolactones via a three-component condensation of isocyanides and acetylenic esters with 2-bromo-1-(4-bromophenyl)ethanone

机译:通过异氰酸酯和炔属酯与2-溴-1-(4-溴苯基)乙酮的三组分缩合反应合成全取代的亚氨基内酯

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摘要

A novel three-component condensation reaction between an isocyanide, an electron-deficient acetylenic ester, and 2-bromo-1-(4-bromophenyl)‐ethanone efficiently provides fully substituted iminolactones in a one-pot condensation reaction without any activation or modification in high yields.
机译:异氰酸酯,缺电子的炔属酯与2-溴-1-(4-溴苯基)-乙酮之间的新型三组分缩合反应可在单锅缩合反应中有效地提供完全取代的亚氨基内酯,而无需任何活化或修饰高产。

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