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Methoxymethylene triphenylphosphorane

Aldehydes can be prepared by the Wittig reaction using (methoxymethylene)-triphenylphosphorane as the Wittig reagent and then hydrolyzing the product with acid. For example,... [Pg.741]

C 6U2IN02S2 35012-51-2) see Timepidium bromide (methoxymethylene)triphenylphosphorane (C2(lH,gOP 20763-19-3) see Glaziovine (7a)-3-methoxy-7-methylcstra-2,5(10)-dicn-17-one 5210-25-3) sec Tibolone... [Pg.2408]

See other pages where Methoxymethylene triphenylphosphorane is mentioned: [Pg.481]    [Pg.77]    [Pg.391]    [Pg.104]    [Pg.375]    [Pg.232]    [Pg.998]    [Pg.120]    [Pg.459]    [Pg.24]    [Pg.30]    [Pg.251]    [Pg.769]    [Pg.104]    [Pg.481]    [Pg.77]    [Pg.391]    [Pg.104]    [Pg.375]    [Pg.232]    [Pg.998]    [Pg.120]    [Pg.459]    [Pg.24]    [Pg.30]    [Pg.251]    [Pg.769]    [Pg.104]   
See also in sourсe #XX -- [ Pg.459 ]



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Methoxymethylene

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