Abstract
The polyhydroxyanthraquinones
known from the crinoid Comatula pectinata are shown to be present largely
as (fish repellent) sulfate monoesters. The sodium salt of the 3-O-sulfate of
4-butyryl-1,3-dihydroxy-6,8-dimethoxy-9,10-anthraquinone was isolated by its
chromatographic mobility on alumina in aqueous acetone or on sodium bicarbonate
in aqueous ethanol. The sulfate hydrolyses readily to the free phenol and is methylated (Me2SO4/K2CO3
in refluxing acetone) to 4-butyryl-1,3,6,8-tetramethoxyanthraquinone.
Methylated in the presence of tertiary alcohols
however, the sulfate ester resists cleavage, yielding the 1,6,8-trimethyl
ether, hydrolysable to 4-butyryl-3-hydroxy-1,6,8-trimethoxyanthraquinone.
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