A process for the preparation of N-debenzoylpaclitaxel (I) through
esterification of 7-protected baccatin III with a carboxylic acid
reactive derivative of general formula (II), and elimination of the
ester-protecting groups in acid conditions and in a single step. In
formula (II) R1 is aryl or heteroaryl. The compound of formula (I) can be
conveniently used for the preparation of paclitaxel and analogues
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