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可见光光氧化还原催化的内酰胺直接N-(杂)芳基化反应

Visible-Light Photoredox Catalytic Direct N-(Het)Arylation of Lactams.

作者信息

Boselli Monica Fiorenza, Ghosh Indrajit, Intini Niccolò, Fattalini Marco, Puglisi Alessandra, König Burkhard, Benaglia Maurizio

机构信息

Dipartimento di Chimica, Università degli Studi di Milano, Via C. Golgi 19, 20133, Milano, Italy.

Fakultät für Chemie und Pharmazie, Universität Regensburg, 93053, Regensburg, Germany.

出版信息

Chemistry. 2025 Mar 25;31(18):e202404385. doi: 10.1002/chem.202404385. Epub 2025 Feb 14.

Abstract

Lactam rings are essential structural motifs in organic chemistry, widely present in natural products and clinically important drugs, such as antibiotics and antiepileptics. Existing methods for synthesizing N-functionalized lactams often require harsh conditions, toxic reagents, or complex catalytic systems. Here, we report a mild and efficient photochemical approach for generating N-centered radicals, enabling straightforward N-heteroarylation of lactams. This versatile method enables the synthesis of a range of N-(het)arylated lactams and is effective even in aqueous media, facilitating the functionalization of biomolecules. Furthermore, the photochemical reaction is easily scalable under continuous flow conditions, making it highly suitable for large-scale applications.

摘要

内酰胺环是有机化学中必不可少的结构基序,广泛存在于天然产物和临床上重要的药物中,如抗生素和抗癫痫药物。现有的合成N-官能化内酰胺的方法通常需要苛刻的条件、有毒试剂或复杂的催化体系。在此,我们报道了一种温和且高效的光化学方法来生成以氮为中心的自由基,从而实现内酰胺的直接N-杂芳基化。这种通用方法能够合成一系列N-(杂)芳基化内酰胺,甚至在水性介质中也有效,便于生物分子的功能化。此外,该光化学反应在连续流动条件下易于放大,非常适合大规模应用。

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