Asymmetric Synthesis of Highly Substituted Spiro[2H-pyrrole-2,3-Succinimide] Derivatives by Copper-Catalyzed Post-Ugi Reactions

IF 4 2区 化学 Q2 CHEMISTRY, APPLIED Advanced Synthesis & Catalysis Pub Date : 2025-04-22 DOI:10.1002/adsc.202500166
Javier Gómez-Ayuso, Israel Carreira-Barral, Roberto Quesada, María García-Valverde
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Abstract

Herein we present a novel one-pot methodology for the synthesis of enantioenriched 2H-pyrrolespirosuccinimides by copper-catalyzed reactions on Ugi adducts derived from enantiopure α-alkylbenzyl amines through a chirality transfer process. We have proposed a mechanism, supported by density functional theory (DFT) calculations, where a hydrogen radical-shuttle (HRS) process explains the chemical and stereochemical results. This work demonstrates the efficient stereoselective synthesis of structurally unique, highly functionalized nitrogen heterocyclic systems using simple protocols and affordable starting materials.

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铜催化后ugi反应合成高取代螺旋[2h -吡咯-2,3-琥珀酰亚胺]衍生物
本文提出了一种新的单通道方法,通过手性转移反应,以铜为催化剂,在对映纯α-烷基苄胺衍生的Ugi加合物上合成对映富集的2h -吡啶螺基琥珀酰亚胺。我们提出了一种由密度泛函理论(DFT)计算支持的机制,其中氢自由基穿梭(HRS)过程解释了化学和立体化学结果。这项工作证明了高效立体选择性合成结构独特,高功能化的氮杂环系统使用简单的协议和负担得起的起始材料。
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来源期刊
Advanced Synthesis & Catalysis
Advanced Synthesis & Catalysis 化学-应用化学
CiteScore
9.40
自引率
7.40%
发文量
447
审稿时长
1.8 months
期刊介绍: Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry. The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.
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