Approach to Geminal Bisperoxides from Aldehydes via BR <sub>3</sub> /O <sub>2</sub> -Enabled Peroxidation

-enabled peroxidation of aldehydes for the selective synthesis of geminal bisperoxides is reported. A range of geminal bisperoxides was obtained in high yields (up to >99%) from simple precursors. The synthetic utility was demonstrated through their diverse transformations into azidoperoxides, cyanoperoxides, peroxyesters, esters, and carboxylic acids. Mechanistic studies support the involvement of a radical pathway.

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Publication Details

Journal
Organic Letters
Published
2026-07-26
DOI
https://doi.org/10.1021/acs.orglett.6c02563
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Approach to Geminal Bisperoxides from Aldehydes via BR 3 /O 2 -Enabled Peroxidation

Do Hyun Ryu, T. SEO, Gyoungho Noh
Organic Letters
Oxidative Organic Chemistry Reactions
article

Approach to Geminal Bisperoxides from Aldehydes via BR 3 /O 2 -Enabled Peroxidation

Do Hyun Ryu, T. SEO, Gyoungho Noh
article en

Abstract

-enabled peroxidation of aldehydes for the selective synthesis of geminal bisperoxides is reported. A range of geminal bisperoxides was obtained in high yields (up to >99%) from simple precursors. The synthetic utility was demonstrated through their diverse transformations into azidoperoxides, cyanoperoxides, peroxyesters, esters, and carboxylic acids. Mechanistic studies support the involvement of a radical pathway.

Organic Letters
Sungkyunkwan University (KR)
Openalex Percentile: Top 16%
Oxidative Organic Chemistry Reactions
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