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Cycloheptatriene anodic oxidation

On the other hand, the anodic oxidation of 1,3,5-cycloheptatrienes is one of the most powerful key tools for the preparation of a variety of non-benzenoid aromatic compounds such as tropylium salts, tropones, tropolones, 2H -cyclohcpta h furan-2-oncs and azulenes14. [Pg.765]

Cycloheptatriene gives 7-methoxycycloheptatriene (13) (7-MCHT) by anodic oxidation in methanol (equation 18). ... [Pg.796]

Although (13) gives benzaldehyde dimethyl acetal (63%) upon further anodic oxidation, 3-methoxy-cycloheptatriene (14) (3-MCHT) and l>meAoxycycloheptatriene (15) (1-MCHT) afford 7,7-dimethoxy cycloheptatriene (16), which is a good precursor of tropone (equation 19). [Pg.796]

See other pages where Cycloheptatriene anodic oxidation is mentioned: [Pg.765]    [Pg.616]    [Pg.765]    [Pg.194]   
See also in sourсe #XX -- [ Pg.796 ]

See also in sourсe #XX -- [ Pg.796 ]

See also in sourсe #XX -- [ Pg.7 , Pg.796 ]

See also in sourсe #XX -- [ Pg.7 , Pg.796 ]

See also in sourсe #XX -- [ Pg.796 ]



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1.3.5- Cycloheptatrien

Anode oxidation

Anodes oxides

Anodic oxidation

Anodic oxides

Cycloheptatriene oxidation

Cycloheptatrienes

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