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.

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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

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article

Practical Povidone Iodine Catalyzed Synthesis of 2,5-Disubstituted Oxazoles from Acetophenones and α-Amino Acids

Jiangmeng Ren, Bu‐Bing Zeng, Jian Wang, Mengfei Li et al.
Synlett
Fluorine in Organic Chemistry
article

Practical Povidone Iodine Catalyzed Synthesis of 2,5-Disubstituted Oxazoles from Acetophenones and α-Amino Acids

Jiangmeng Ren, Bu‐Bing Zeng, Jian Wang, Mengfei Li, Xueqin Sun, Shaodong Wang
article en

Abstract

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.

SynlettVol. 36(08)
Shanghai Municipal Education Commission
Openalex Percentile: Top 100%
Fluorine in Organic Chemistry
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