首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A convenient method for synthesis of polyfunctional dihydropyrrole spiro-fused oxindole-2-ones via an organocatalytic tandem Michael/cyclization sequence
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A convenient method for synthesis of polyfunctional dihydropyrrole spiro-fused oxindole-2-ones via an organocatalytic tandem Michael/cyclization sequence

机译:一种通过有机催化串联迈克尔/环化序列合成多官能二氢吡咯螺旋稠合的羟吲哚-2-酮的简便方法

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摘要

A new methodology was developed for the synthesis of spirocyclic oxindoles bearing polyfunctional dihydropyrrole units via an organocatalytic tandem Michaelicyclization sequence. Products bearing adjacent quaternary-tertiary stereocenters were smoothly obtained in high yields (up to 97% yield) with excellent diastereoselectivities up to >20/1. (C) 2014 Elsevier Ltd. All rights reserved.
机译:开发了一种新的方法,用于通过有机催化串联米氏环化序列合成带有多官能二氢吡咯单元的螺环羟吲哚。以高收率(高达97%的收率)和高达> 20/1的优异非对映选择性,可以平稳地获得带有相邻四级-三级立体中心的产物。 (C)2014 Elsevier Ltd.保留所有权利。

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