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通过协同烯胺、光氧化还原和钴三重催化合成芳香醛的去饱和方法。

A Desaturative Approach for Aromatic Aldehyde Synthesis via Synergistic Enamine, Photoredox and Cobalt Triple Catalysis.

作者信息

Zhao Huaibo, Caldora Henry P, Turner Oliver, Douglas James J, Leonori Daniele

机构信息

Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.

Oncology R&DI Medicinal Chemistry, AstraZeneca, Darwin Building, Unit 310, Cambridge Science Park, Milton Road, Cambridge, CB4 0WG, UK.

出版信息

Angew Chem Int Ed Engl. 2022 Apr 25;61(18):e202201870. doi: 10.1002/anie.202201870. Epub 2022 Mar 9.

DOI:10.1002/anie.202201870
PMID:35196413
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9311220/
Abstract

Aromatic aldehydes are fundamental intermediates that are widely utilised for the synthesis of important materials across the broad spectrum of chemical industries. Accessing highly substituted derivatives can often be difficult as their functionalizations are generally performed via electrophilic aromatic substitution, S Ar. Here we provide an alternative and mechanistically distinct approach whereby aromatic aldehydes are assembled from saturated precursors via a desaturative process. This novel strategy harnesses the high-fidelity of Diels-Alder cycloadditions to quickly construct multi-substituted cyclohexenecarbaldehyde cores which undergo desaturation via the synergistic interplay of enamine, photoredox and cobalt triple catalysis.

摘要

芳香醛是重要的中间体,广泛应用于化学工业各个领域中重要材料的合成。由于其官能化通常通过亲电芳香取代反应(S Ar)进行,因此获得高度取代的衍生物往往具有挑战性。在此,我们提供了一种替代的、机理不同的方法,即通过去饱和过程从饱和前体组装芳香醛。这种新策略利用狄尔斯-阿尔德环加成反应的高保真度,快速构建多取代的环己烯甲醛核心,该核心通过烯胺、光氧化还原和钴三重催化的协同作用进行去饱和反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/9311220/4cba0d373c8a/ANIE-61-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/9311220/6458cb369ad4/ANIE-61-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/9311220/543538dd94ca/ANIE-61-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/9311220/4cba0d373c8a/ANIE-61-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/9311220/6458cb369ad4/ANIE-61-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/9311220/543538dd94ca/ANIE-61-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/9311220/4cba0d373c8a/ANIE-61-0-g003.jpg

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