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Prelog-Djerassi lactonic acid, methyl ester

Synthetic Application ( + )-Prelog-Djerassi Lactonic Acid Methyl Ester. . 25... [Pg.1]

Another interesting way to construct 8-lactones is the Baeyer-Villiger oxidation [72] of cyclopentanones. For example, Hacini and Santelli have reported an efficient synthesis of the Prelog-Djerassi lactone methyl ester using Baeyer-Villiger oxidation [73] (Scheme 30). Hydrolysis of enol ether 162 derived from —)-trans-pulegenic acid furnished an inseparable diastereomeric mixture of the corresponding dimethylacetals. Ozonolysis of the olefin and subsequent... [Pg.114]

See other pages where Prelog-Djerassi lactonic acid, methyl ester is mentioned: [Pg.205]    [Pg.25]    [Pg.25]    [Pg.205]    [Pg.25]    [Pg.25]    [Pg.270]    [Pg.54]   


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Esters lactones

Lactone esters

Lactones acid esters)

Prelog

Prelog-Djerassi lactone

Prelog-Djerassi lactonic acid

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