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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >One-pot synthesis of pentasubstituted pyrroles from propargylic alcohols, amines, and dialkyl acetylenedicarboxylates; Tandem amination, propargylation and cycloisomerization catalyzed by molecular iodine
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One-pot synthesis of pentasubstituted pyrroles from propargylic alcohols, amines, and dialkyl acetylenedicarboxylates; Tandem amination, propargylation and cycloisomerization catalyzed by molecular iodine

机译:由炔丙醇,胺和乙炔二羧酸二烷基酯一锅法合成五取代的吡咯;分子碘催化的串联胺化,炔丙基化和环异构化

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摘要

A multicomponent one-pot synthesis of fully substituted pyrroles has been developed by the tandem reaction of amines, dialkyl acetylenedicarboxylates, and propargylic alcohols using iodine as a catalyst. The reaction was complete in three hours and afforded the products in high yields (75-88%). The method is simple, efficient, cost-effective, and metal-free.
机译:通过使用碘作为催化剂的胺,乙炔二羧酸二烷基酯和炔丙醇的串联反应,已经开发了全取代吡咯的多组分一锅合成法。反应在三小时内完成,并以高收率(75-88%)提供产物。该方法简单,有效,具有成本效益并且不含金属。

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