Griesbaum coozonolysis
The Griesbaum coozonolysis is a name reaction in organic chemistry that allows for the preparation of tetrasubstituted ozonides (1,2,4-trioxolanes) by the reaction of O-methyl oximes with a carbonyl compound in the presence of ozone. Contrary to their usual roles as intermediates in ozonolysis and other oxidative alkene cleavage reactions, 1,2,4-trioxolanes are relatively stable compounds and are isolable.
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Griesbaum coozonolysis
The Griesbaum coozonolysis is a name reaction in organic chemistry that allows for the preparation of tetrasubstituted ozonides (1,2,4-trioxolanes) by the reaction of O-methyl oximes with a carbonyl compound in the presence of ozone. Contrary to their usual roles as intermediates in ozonolysis and other oxidative alkene cleavage reactions, 1,2,4-trioxolanes are relatively stable compounds and are isolable.
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The Griesbaum coozonolysis is ...... le compounds and are isolable.
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name
Griesbaum coozonolysis
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namedafter
Karl Griesbaum
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type
Organic redox reaction
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The Griesbaum coozonolysis is ...... le compounds and are isolable.
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label
Griesbaum coozonolysis
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