Annulative endoperoxidation of tetronates

A novel, annulative endoperoxidation of tetronate derivatives bearing unsaturated side chains is presented. The reaction requires a simple setup and proceeds under mild conditions to generate tricyclic endoperoxides in modest diastereoselectivities and useful yields. A free-radical mechanism is proposed.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00663e
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Annulative endoperoxidation of tetronates

Marat R. Talipov, Rodolfo Tello‐Aburto, Cory J. Windorff, Najmeh Rahimi et al.
Organic & Biomolecular Chemistry
Oxidative Organic Chemistry Reactions
article

Annulative endoperoxidation of tetronates

Marat R. Talipov, Rodolfo Tello‐Aburto, Cory J. Windorff, Najmeh Rahimi, Bayler G. Barnes, Saba Sehrish, Samuel K. Akompong
article en

Abstract

A novel, annulative endoperoxidation of tetronate derivatives bearing unsaturated side chains is presented. The reaction requires a simple setup and proceeds under mild conditions to generate tricyclic endoperoxides in modest diastereoselectivities and useful yields. A free-radical mechanism is proposed.

Organic & Biomolecular ChemistryVol. 23(34)
New Mexico State University (US)
New Mexico State University, National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 85%
Oxidative Organic Chemistry Reactions
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