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Esters 1a, 1d and 1e are commercially available. Esters 1b and 1c were prepared respectively from 4-methylpentanoic acid and tert-butanol using DIC/DMAP in 39% yield and from 4-phenylbutyric acid chloride and potassium tert-butylate in 74% yield
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Esters 1a, 1d and 1e are commercially available. Esters 1b and 1c were prepared respectively from 4-methylpentanoic acid and tert-butanol using DIC/DMAP in 39% yield and from 4-phenylbutyric acid chloride and potassium tert-butylate in 74% yield.
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