8 citations as recorded by crossref.

1. Conformation-specific reactions of Criegee intermediates C. Chung et al. https://doi.org/10.1063/5.0278251
2. Infrared Spectrum of the Adduct 2-Chloro-2-hydroperoxybut-3-ene [(C2H3)CCl(CH3)OOH] of the Reaction between the Criegee Intermediate Methyl Vinyl Ketone Oxide [C2H3C(CH3)OO] and HCl H. Wang & Y. Lee https://doi.org/10.1021/acs.jpca.4c04936
3. Interfacial Extraction to Trap and Characterize the Criegee Intermediates from Phospholipid Ozonolysis J. He et al. https://doi.org/10.1021/acs.analchem.2c05472
4. Ab initio prediction for product stereo-specificity in the CH3CHI + O2 reaction: formation of syn- vs anti-CH3CHOO H. Trac et al. https://doi.org/10.1007/s00894-025-06426-4
5. Criegee Intermediate as a Major Atmospheric Sink for Methane Sulfonamide: A Pathway to Functionalized Hydroperoxides S. Ibrahim J et al. https://doi.org/10.1021/acs.est.5c14460
6. Criegee Intermediate-Mediated Oxidation of Dimethyl Disulfide: Effect of Formic Acid and Its Atmospheric Relevance G. Babu et al. https://doi.org/10.1021/acs.jpca.3c04730
7. Functionalized Hydroperoxide Formation from the Reaction of Methacrolein-Oxide, an Isoprene-Derived Criegee Intermediate, with Formic Acid: Experiment and Theory M. Vansco et al. https://doi.org/10.3390/molecules26103058
8. Temperature-Dependent Kinetics of the Methyl Vinyl Ketone Oxide Criegee Intermediate: Self-Reaction and Reaction with Trifluoroacetic Acid S. Khodia et al. https://doi.org/10.1021/acs.jpca.6c01738