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.
Authors
- Tricia Naicker (ORCID: https://orcid.org/0000-0002-7134-6258)
- Hendrik Gerhardus Kruger (ORCID: https://orcid.org/0000-0003-0606-2053)
- Thavendran Govender (ORCID: https://orcid.org/0000-0003-2511-2503)
- Per I. Arvidsson (ORCID: https://orcid.org/0000-0002-9453-6812)
- Glenn E. M. Maguire (ORCID: https://orcid.org/0000-0002-9135-5370)
- Lloyd C. Chetty (ORCID: https://orcid.org/0000-0002-7343-9781)
Institutions
- University of Zululand (ZA)
- Science for Life Laboratory (SE)
- Karolinska Institutet (SE)
- University of KwaZulu-Natal (ZA)
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
Funders
- National Research Foundation
- Inyuvesi Yakwazulu-Natali