Practical Povidone Iodine Catalyzed Synthesis of 2,5-Disubstituted Oxazoles from Acetophenones and α-Amino Acids
Abstract Nonharmful povidone iodine (PVP-I) was applied in the cyclization of acetophenones and α-amino acids to give 2,5-disubstituted oxazoles. Acetophenones with different substituents and natural α-amino acids were applied to our developed method, and more than 38 2,5-disubstituted oxazole compounds were obtained in moderate to good yields. Several naturally active 5-(3-indolyl)oxazole alkaloids such as pimprinine, labradorin, and pimprinol were successfully acquired in moderate yields using this strategy.
Authors
- Jiangmeng Ren
- Bu‐Bing Zeng (ORCID: https://orcid.org/0000-0002-2709-1497)
- Jian Wang (ORCID: https://orcid.org/0000-0003-4377-4287)
- Mengfei Li (ORCID: https://orcid.org/0000-0003-3035-4427)
- Xueqin Sun
- Shaodong Wang (ORCID: https://orcid.org/0000-0002-7982-6600)
Publication Details
- Journal
- Synlett
- Published
- 2025-01-10
- DOI
- https://doi.org/10.1055/s-0043-1775426
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Shanghai Municipal Education Commission