Iodine-Catalyzed Carbonyl Desaturation: A One-Pot Synthesis of Flavones

-Michael addition. This protocol is a metal-free approach to carbonyl desaturation with nontoxic DMSO as both the solvent and oxidant, which is especially beneficial for the synthesis of pharmaceutical compounds. Mechanistic studies suggest that the transformation proceeds via a radical pathway.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-07-26
DOI
https://doi.org/10.1021/acs.joc.6c01237
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
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0.00
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article

Iodine-Catalyzed Carbonyl Desaturation: A One-Pot Synthesis of Flavones

Bao‐Yin Zhao, Yue Wang, Li-Gang Kou, Bin-Xuan Zou et al.
The Journal of Organic Chemistry
Oxidative Organic Chemistry Reactions
article

Iodine-Catalyzed Carbonyl Desaturation: A One-Pot Synthesis of Flavones

Bao‐Yin Zhao, Yue Wang, Li-Gang Kou, Bin-Xuan Zou, Heng-Xin Mao
article en

Abstract

-Michael addition. This protocol is a metal-free approach to carbonyl desaturation with nontoxic DMSO as both the solvent and oxidant, which is especially beneficial for the synthesis of pharmaceutical compounds. Mechanistic studies suggest that the transformation proceeds via a radical pathway.

The Journal of Organic Chemistry
Ministry of Education of the People's Republic of China (CN)
Openalex Percentile: Top 16%
Oxidative Organic Chemistry Reactions
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Iodine-Catalyzed Carbonyl Desaturation: A One-Pot Synthesis of Flavones — Bao‐Yin Zhao, Yue Wang, et al. · The Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS