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Photooxidation electron-withdrawing groups

FuithemuHe, the presence of electron-withdrawing substituents, such as an allylic hydroxy group, is deactivating, an effect intensified by esterification to a degree such that acylation of an allylic alcohol may be sufficient to protect the double bond during photooxidation at another site. ... [Pg.98]

See other pages where Photooxidation electron-withdrawing groups is mentioned: [Pg.543]    [Pg.543]    [Pg.130]    [Pg.520]    [Pg.209]    [Pg.334]    [Pg.422]    [Pg.531]    [Pg.21]    [Pg.349]   


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