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Stereoselective synthesis of functionalized pyrrolidines by the diverted NH insertion reaction of metallocarbenes with β-aminoketone derivatives

机译:茂金属与β-氨基酮衍生物的转移NH插入反应立体选择性合成官能化吡咯烷

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摘要

A highly stereoselective route to functionalized pyrrolidines from the metal catalyzed diverted N-H insertion of a range of diazocarbonyl compounds with β-aminoketone derivatives is described. A number of catalysts (rhodium(II) carboxylate dimers, copper(I) triflate and an iron(III)porphyrin) are shown to promote the process under mild conditions to give a wide range of highly substituted proline derivatives. The reaction starts with a metallocarbene N-H insertion but is diverted by an intermolecular aldol reaction.
机译:描述了从一系列重氮羰基化合物与β-氨基酮衍生物的金属催化的转移N-H插入到官能化吡咯烷的高度立体选择性的途径。已显示出许多催化剂(羧酸铑(II)二聚体,三氟甲磺酸铜(I)和卟啉铁(III))在温和条件下促进了该过程,从而提供了多种高度取代的脯氨酸衍生物。该反应以金属碳烯N-H插入开始,但通过分子间的醇醛缩合反应转移。

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