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When /ran.v-2-methoxycyclohexyl phenyl tellurium was treated with 2 molar equivalents of sodium periodate in aqueous methanol, formylcyclopentane was isolated in 75% yield. /ram-2-Methoxycycloheptyl phenyl tellurium and an excess of sodium periodate, hydrogen peroxide, or /er/.-butyl hydroperoxide in aqueous methanol produced mixtures of the dimethyl acetal of formylcyclohexane, cyclohexylformaldehyde, and methoxy-2-cyclo-heptene3. [Pg.488]

See other pages where Methoxycycloheptyl phenyl is mentioned: [Pg.431] [Pg.645] [Pg.431] [Pg.645] [Pg.431] [Pg.645] [Pg.431] [Pg.645]

See also in sourсe #XX -- [ Pg.547 ]

See also in sourсe #XX -- [ Pg.547 ]