The alkyl ester may be a C1-6 alkyl ester of an aliphatic hydroxy carboxylic acid having 2-7 carbon atoms, such as a 4-hydroxybutyric acid C1-4 alkyl ester.
An optically active tetrahydrofuranthiocarboxylic acid is converted to an alkyl ester and this ester is analyzed by chromatography with an optically active column.
The organic electrolyte contains 0.0008-1.2% by weight of an alkyl ester of an aliphatic hydroxy carboxylic acid.
The resulting protected alkyl ester alkyl ketoside is then alkylated at the C-4 position whereby the hydrogen of the C-4 hydroxyl group is replaced with an alkyl group to form an alkoxy group.
The present invention concerns the use as perfuming ingredient of a lower alkyl ester of 4,6,6-trimethyl-1,3-cyclohexadiene-1-carboxylate or 4,6,6-trimethyl-3-cyclohexene-1-carboxylate.
The present invention is related to lower alkyl 10,20 di-O-ester derivatives of camptothecins and pharmaceutical formulations thereof.
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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