Synthesis of side chain modified apicidin derivatives: potent mechanism-based histone deacetylase inhibitors
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文摘
An efficient degradation of apicidin's ketone-containing side chain to two common intermediates (the C7-aldehyde and the C8-methyl ester) is described. From these intermediates, a series of potent mechanism-based histone deacetylase inhibitors was prepared to facilitate biochemical studies.

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