Oxygen–Oxygen Bond-Forming Reactions for the Synthesis of Cyclic Peroxides

O-labeling experiments and by the determination that the reaction proceeds with retention of configuration at the carbon atoms of the ring. The reaction was rapid at -78 °C, it was high-yielding, and it was general for a range of substrates, including the formation of five- and six-membered cyclic and bicyclic peroxides. This reaction, therefore, serves as a synthetic analogy to the oxygen-oxygen bond formation reaction used in nature to form dioxygen.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-05-08
DOI
https://doi.org/10.1021/jacs.6c04588
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Oxygen–Oxygen Bond-Forming Reactions for the Synthesis of Cyclic Peroxides

K A Woerpel, Elena J. Helm, Farhan A. Chowdhury
Journal of the American Chemical Society
Oxidative Organic Chemistry Reactions
article

Oxygen–Oxygen Bond-Forming Reactions for the Synthesis of Cyclic Peroxides

K A Woerpel, Elena J. Helm, Farhan A. Chowdhury
article en

Abstract

O-labeling experiments and by the determination that the reaction proceeds with retention of configuration at the carbon atoms of the ring. The reaction was rapid at -78 °C, it was high-yielding, and it was general for a range of substrates, including the formation of five- and six-membered cyclic and bicyclic peroxides. This reaction, therefore, serves as a synthetic analogy to the oxygen-oxygen bond formation reaction used in nature to form dioxygen.

Journal of the American Chemical Society
New York University (US)
NIH Office of the Director, National Institute of General Medical Sciences, Division of Chemistry
Openalex Percentile: Top 10%
Oxidative Organic Chemistry Reactions
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