Tryptophan-replacement and indole-modified apicidins: synthesis of potent and selective antiprotozoal agents
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文摘
A ruthenium tetraoxide catalyzed degradation of apicidin's tryptophan indole provided access to two useful carboxylic acid homolog intermediates. The synthesis of a series of potent and/or selective ketone homologs and 2-arylindoles derived from apicidin is described.

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