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Mechanism of Ozonolysis
Angewandte Chemie International Edition in English · 1975 · Vol. 14(11) · pp. 745–752
Abstract
Abstract The formation of ozonides (1,2,4‐trioxolanes) from alkenes and ozone can be described as a succession of three [2+3] cycloadditions or cycloreversions involving primary ozonides (1,2,3‐trioxolanes) and aldehyde or ketone oxides as decisive intermediates, all of which have finite lifetimes. There is no warranted experimental basis for assuming an alternative mechanism.
Chemical Reactions and MechanismsClick Chemistry and ApplicationsFluorine in Organic ChemistryOzonolysisAldehydeMechanism (biology)KetoneOzoneReaction mechanismChemistryPrimary (astronomy)Computational chemistryOrganic chemistry
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Cited by
Catalytic ozonation for water and wastewater treatment: Recent advances and perspective
The Science of The Total Environment · 2019 · 1,049 citations
References
1,3‐Dipolar Cycloadditions. Past and Future
Angewandte Chemie International Edition in English · 1963 · 2,816 citations
1.3‐Dipolare Cycloadditionen Rückschau und Ausblick
Angewandte Chemie · 1963 · 1,296 citations
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