Pd/Ag-Cocatalyzed Merging Intramolecular Oxidative Coupling and Cascade [4 + 2] Cycloaddition: Synthesis and Photophysical Properties of Novel Polycyclic N-Heterocycles Fused Naphthoquinones

We report a step-economic strategy for the direct synthesis of novel polycyclic <i>N</i>-heterocycle-fused naphthoquinones by merging intramolecular oxidative coupling and cascade [4 + 2] cycloaddition. In the protocol, mechanistic investigations suggest that the cascade reaction involves the intermediate spiro polycyclic <i>N</i>-heterocycles and [4 + 2] cycloaddition processes. This protocol is featured with moderate to excellent yields, wide substrate scope, and divergent structures of products. In addition, the photophysical properties of the synthesized products were evaluated. These products exhibit interesting fluorescence properties, and surprisingly, the compounds have the ability to selectively recognize trifluoroacetic acid.

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Publication Details

Journal
Molecules
Published
2024-11-28
DOI
https://doi.org/10.3390/molecules29235639
Citations
1
Primary Topic
Bioactive Compounds and Antitumor Agents
Type
article
Field-Weighted Citation Impact
0.35
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article

Pd/Ag-Cocatalyzed Merging Intramolecular Oxidative Coupling and Cascade [4 + 2] Cycloaddition: Synthesis and Photophysical Properties of Novel Polycyclic N-Heterocycles Fused Naphthoquinones

Han-Qing Wu, Lin Chen, Yurong Liu, Zhifan Wang et al.
1 citations
Molecules
Bioactive Compounds and Antitumor Agents
0.35
article

Pd/Ag-Cocatalyzed Merging Intramolecular Oxidative Coupling and Cascade [4 + 2] Cycloaddition: Synthesis and Photophysical Properties of Novel Polycyclic N-Heterocycles Fused Naphthoquinones

Han-Qing Wu, Lin Chen, Yurong Liu, Zhifan Wang, Fan Yang, Guowei Deng, Jianjin Yu, Yuting Wang, Yu Dong, Li Xie
article en
1 citations

Abstract

We report a step-economic strategy for the direct synthesis of novel polycyclic <i>N</i>-heterocycle-fused naphthoquinones by merging intramolecular oxidative coupling and cascade [4 + 2] cycloaddition. In the protocol, mechanistic investigations suggest that the cascade reaction involves the intermediate spiro polycyclic <i>N</i>-heterocycles and [4 + 2] cycloaddition processes. This protocol is featured with moderate to excellent yields, wide substrate scope, and divergent structures of products. In addition, the photophysical properties of the synthesized products were evaluated. These products exhibit interesting fluorescence properties, and surprisingly, the compounds have the ability to selectively recognize trifluoroacetic acid.

MoleculesVol. 29(23)
Chengdu Center for Disease Control and Prevention (CN), Chengdu Normal University (CN)
Openalex Percentile: Top 39%
Bioactive Compounds and Antitumor Agents
0.35
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