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Phenylvaleric Acid and Cognate Acids

Synthesis of this acid is less demanding (Reaction scheme 187), and therefore only a few alternatives appeared in the patent hterature. [Pg.97]

This principle was applied to similar variations [520]. Production of pure benzyl chlorides sometimes poses a technical problem, giving a reason for better proposals [521]. [Pg.97]

More exotic methods are chemically interesting, for example the oxidative rearrangement of phenylalkylketones 264 (Reaction scheme 188) with thalliumnitrate in orthoester as the solvent [522]. [Pg.97]

Arylalkyl ketones rearrange on treatment with phosphoryl azides to give the phosphorylated amide of fenvaleric acid (Reaction scheme 191) [526]. [Pg.98]

A close analogue is the acid 267 for flucythrinate. Some methods of preparing the 4-difluoromethoxyphenyl isovaleric 267 acid are described in Reaction scheme 192  [Pg.98]


See other pages where Phenylvaleric Acid and Cognate Acids is mentioned: [Pg.96]    [Pg.97]    [Pg.99]   


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7-Phenylvaleric acid

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