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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of 4-Hydroxy-lH-pyrrole-2,3-dicarboxylic Acid Derivatives: Unusual Coupling of Acetylenic Esters and a-Amino Acids in the Presence of Cyclohexyl Isocyanide or N,N'-Dicyclohexylcarbodiimide
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Synthesis of 4-Hydroxy-lH-pyrrole-2,3-dicarboxylic Acid Derivatives: Unusual Coupling of Acetylenic Esters and a-Amino Acids in the Presence of Cyclohexyl Isocyanide or N,N'-Dicyclohexylcarbodiimide

机译:4-羟基-1H-吡咯-2,3-二羧酸衍生物的合成:在环己基异氰化物或N,N'-二环己基碳二亚胺存在下,乙酰酯和α-氨基酸的异常偶联

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摘要

A facile and direct synthetic entry to 4-hydroxy-1 H-pyr-role-2,3-dicarboxylic acid derivatives is reported. It is based on the unusual ring annulation of acetylenic esters and alpha-amino acids with isocyanide or carbodiimide under neutral conditions in a one-step procedure.
机译:据报道,一种容易且直接的合成进入4-羟基-1 H-pyr-role-2,3-二羧酸衍生物。它是基于炔醇酯和α-氨基酸与异氰酸酯或碳二亚胺在中性条件下以一步法进行的异常环环化。

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