Abstract
New D-seco-taxoids were synthesized from 1-deoxybaccatin VI and their structures were confirmed by 1H NMR, 13C NMR, ESIMS and X-ray crystallography. The key step of the synthesis involved the opening of the oxetane ring under acid and basic conditions in order to obtain new multidrug resistance (MDR) reversal agents and new synthetic precursors of paclitaxel analogues.
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