Sl. Colletti et al., Tryptophan-replacement and indole-modifed apicidins: synthesis of potent and selective antiprotozoal agents, TETRAHEDR L, 41(41), 2000, pp. 7825-7829
A ruthenium tetraoxide catalyzed degradation of apicidin's tryptophan indol
e provided access to two useful carboxylic acid homolog intermediates. The
synthesis of a series of potent and/or selective ketone homologs and 2-aryl
indoles derived from apicidin is described. (C) 2000 Elsevier Science Ltd.
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