The Oxidation of Electron-Rich Arenes Using a H<sub>2</sub>O<sub>2</sub>–Proline System

This study introduces a novel proline-catalyzed oxidation system employing hydrogen peroxide to synthesize quinones from a diverse range of substrates, including hydroquinones, phenols, resorcinols, aldehydes, and polycyclic aromatics. This approach is well-aligned with green chemistry principles, offering a more environmentally benign approach than earlier studies. Notably, this approach uses cost-effective reagents, proline as a readily available organocatalyst, reduced equivalents of H<sub>2</sub>O<sub>2</sub>, metal-free conditions, and notably short reaction times to achieve moderate-to-high yields. This promising approach encourages further exploration of the H<sub>2</sub>O<sub>2</sub>-proline system in oxidation reactions. This study's innovative approach and good results set a strong foundation for future research to expand the scope and efficiency of green oxidation processes.

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Publication Details

Journal
ACS Omega
Published
2024-08-22
DOI
https://doi.org/10.1021/acsomega.4c04383
Citations
1
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.25

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The Oxidation of Electron-Rich Arenes Using a H2O2–Proline System

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ACS Omega
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article

The Oxidation of Electron-Rich Arenes Using a H2O2–Proline System

Tricia Naicker, Hendrik Gerhardus Kruger, Thavendran Govender, Per I. Arvidsson, Glenn E. M. Maguire, Lloyd C. Chetty
article en
1 citations

Abstract

This study introduces a novel proline-catalyzed oxidation system employing hydrogen peroxide to synthesize quinones from a diverse range of substrates, including hydroquinones, phenols, resorcinols, aldehydes, and polycyclic aromatics. This approach is well-aligned with green chemistry principles, offering a more environmentally benign approach than earlier studies. Notably, this approach uses cost-effective reagents, proline as a readily available organocatalyst, reduced equivalents of H<sub>2</sub>O<sub>2</sub>, metal-free conditions, and notably short reaction times to achieve moderate-to-high yields. This promising approach encourages further exploration of the H<sub>2</sub>O<sub>2</sub>-proline system in oxidation reactions. This study's innovative approach and good results set a strong foundation for future research to expand the scope and efficiency of green oxidation processes.

ACS OmegaVol. 9(35)
University of Zululand (ZA), Science for Life Laboratory (SE), Karolinska Institutet (SE), University of KwaZulu-Natal (ZA)
National Research Foundation, Inyuvesi Yakwazulu-Natali
Openalex Percentile: Top 49%
Oxidative Organic Chemistry Reactions
0.25
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