Lithium perchlorate-catalysed rearrangement of 1-methylcyclohex-2-enylhydroperoxide into 2-methylenecyclohexylhydroperoxide

SummaryThis review is the first to collate and summarize main data on named and unnamed rearrangement reactions of peroxides. It should be noted, that in the chemistry of peroxides two types of processes are considered under the term rearrangements. These are conventional rearrangements occurring with the retention of the molecular weight and transformations of one of the peroxide moieties after O–O-bond cleavage. Detailed information about the Baeyer−Villiger, Criegee, Hock, Kornblum−DeLaMare, Dakin, Elbs, Schenck, Smith, Wieland, and Story reactions is given. Unnamed rearrangements of organic peroxides and related processes are also analyzed. The rearrangements and related processes of important natural and synthetic peroxides are discussed separately.

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Lithium perchlorate-catalysed rearrangement of 1-methylcyclohex-2-enylhydroperoxide into 2-methylenecyclohexylhydroperoxide

Cited by 3 publications

References 9 publications

Thermodynamic and physicochemical properties of binary mixtures of nitromethane with {2-methoxyethanol+2-butoxyethanol} systems at T=(293.15, 298.15, 303.15, 308.15, and 313.15)K

Thermodynamic and physicochemical properties of binary mixtures of nitromethane with {2-methoxyethanol+2-butoxyethanol} systems at T=(293.15, 298.15, 303.15, 308.15, and 313.15)K

Studies on the intermolecular interactions in the binary mixtures of nitrobenzene with 2-methoxyethanol, 2-ethoxyethanol, 2-propoxyethanol and 2-butoxyethanol atT = 298.15 K

Rearrangements of organic peroxides and related processes

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