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PREVOST-WOODWARD Olefin Hydroxylation

Vicinal iodo carboxylates may also be prepared from the reaction of olefins either with iodine and potassium iodate in acetic acid/ or with N-iodosuccinimide and a carboxylic acid in chloroform. " A number of new procedures for effecting the hydroxylation or acyloxylation of olefins in a manner similar to the Prevost or Woodward-Prevost reactions include the following iodo acetoxylation with iodine and potassium chlorate in acetic acid followed by acetolysis with potassium acetate reaction with iV-bromoacetamide and silver acetate in acetic acid reaction with thallium(III) acetate in acetic acid and reaction with iodine tris(trifluoroacetate) in pentane. ... [Pg.88]

See other pages where PREVOST-WOODWARD Olefin Hydroxylation is mentioned: [Pg.226]    [Pg.294]    [Pg.226]    [Pg.226]    [Pg.294]    [Pg.226]    [Pg.294]    [Pg.226]    [Pg.226]    [Pg.294]    [Pg.670]   
See also in sourсe #XX -- [ Pg.305 ]



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Olefins hydroxylation

PREVOST WOODWARD Olefin

Prevost, hydroxylation

Woodward

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