Synthesis of unstrained Criegee intermediates: inverse α-effect and other protective stereoelectronic forces can stop Baeyer-Villiger rearrangement of γ-hydroperoxy-γ-peroxylactones.

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

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Who cites it

5 citing papers in PubMed.

1. Bridged 1,2,4-Trioxolanes: SnClMolecules (Basel, Switzerland) · 2023
   Article
2. Lewis Acids and Heteropoly Acids in the Synthesis of Organic Peroxides.Pharmaceuticals (Basel, Switzerland) · 2022
   Review
3. Criegee Intermediates Beyond Ozonolysis: Synthetic and Mechanistic Insights.Angewandte Chemie (International ed. in English) · 2021
   Review
4. Stalling chromophore synthesis of the fluorescent protein Venus reveals the molecular basis of the final oxidation step.Chemical science · 2021
   Article
5. Application of BFChemistry of heterocyclic compounds · 2020
   Article

Corrections and comments

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Authors and funding

8 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

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