摘要 |
<p>The invention comprises a novel process for the preparation of an epothilone derivative of formula I: wherein R<SUP>1 </SUP>and R<SUP>2 </SUP>independently from each other represent hydrogen or protecting groups and R<SUP>3 </SUP>is methyl or trifluoromethyl, which are useful precursors in the synthesis of the desoxyepothilone derivatives of the formula IV: wherein R<SUP>3 </SUP>is methyl or trifluoromethyl. The desoxepothilones of formula IV inhibit the growth of tumor cells and are therefore promising candidates for novel anticancer agents.</p> |