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Criegee glycol oxidation

Other references related to the Criegee glycol oxidation are cited in the literature. [Pg.763]

This reaction is related to the Criegee Glycol Oxidation. [Pg.1808]

The mechanism of glycol oxidation with Pb(OAc)4 was proposed by Criegee ... [Pg.1520]

Criegee, R. Oxidation with quadrivalent lead salts. II. Oxidative cleavage of glycols. Ber. 1931, 64B, 260-266. [Pg.568]

Criegee reaction. Oxidative cleavage of vicinal glycols by lead tetraacetate. [Pg.345]

Criegee glycol cleavage reaction Subtractive oxidation... [Pg.292]

The exact course of the periodate reaction has not yet been established. That an intermediate complex, compound, or ion is involved has been determined kinetically.28 269 261 262 283-286 The exact structure of this intermediate is still in doubt. The most universally accepted structure is a cyclic ester intermediate propounded by Criegee,27 285 analogous to his cyclic ester intermediate for another agent oxidizing 1,2-glycols, lead tetraacetate. [Pg.40]

Criegee oxidation Cleavage of 1,2-diols (glycols) to the corresponding carbonyl compounds using LTA. 114... [Pg.511]

Osmic esters of type (I) are intermediates in Hofmann oxidation of olefins and they have been isolated by Criegee.122 They are cleaved to glycols by... [Pg.289]

See other pages where Criegee glycol oxidation is mentioned: [Pg.14]    [Pg.389]    [Pg.14]    [Pg.389]    [Pg.761]    [Pg.762]    [Pg.762]    [Pg.764]    [Pg.1807]    [Pg.14]    [Pg.389]    [Pg.14]    [Pg.389]    [Pg.761]    [Pg.762]    [Pg.762]    [Pg.764]    [Pg.1807]    [Pg.23]    [Pg.128]    [Pg.128]    [Pg.359]    [Pg.11]    [Pg.24]    [Pg.24]    [Pg.36]    [Pg.48]    [Pg.388]    [Pg.584]    [Pg.708]    [Pg.25]    [Pg.209]    [Pg.114]    [Pg.114]    [Pg.409]    [Pg.1113]    [Pg.78]    [Pg.71]    [Pg.584]    [Pg.4038]    [Pg.187]    [Pg.193]    [Pg.761]    [Pg.708]   
See also in sourсe #XX -- [ Pg.14 , Pg.389 ]

See also in sourсe #XX -- [ Pg.76 ]

See also in sourсe #XX -- [ Pg.14 , Pg.389 ]

See also in sourсe #XX -- [ Pg.76 ]



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