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Catecholate, secondary bonding

Phenol was hydroxylated with TS-1 and hydrogen peroxide to give a 1 1 mixture of catechol (4) and hydroquinone (5) (Eqn. 21.6).26>29 Anisole and other substituted benzenes gave similar results. Secondary and tertiary aliphatic C-H bonds were oxidized to give alcohols and ketones, but primary C-H bonds were... [Pg.553]

See other pages where Catecholate, secondary bonding is mentioned: [Pg.438]    [Pg.115]    [Pg.791]    [Pg.33]    [Pg.138]    [Pg.215]    [Pg.184]    [Pg.702]    [Pg.1571]    [Pg.609]    [Pg.438]    [Pg.515]    [Pg.110]    [Pg.123]   
See also in sourсe #XX -- [ Pg.15 , Pg.18 , Pg.19 ]



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Catechol

Catecholate

Secondary bonding

Secondary bonds

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