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Merck

A formal total synthesis of taxol aided by an automated synthesizer.

Chemistry, an Asian journal (2007-04-19)
Takayuki Doi, Shinichiro Fuse, Shigeru Miyamoto, Kazuoki Nakai, Daisuke Sasuga, Takashi Takahashi
ABSTRACT

A 36-step synthesis was carried out in automated synthesizers to provide a synthetic key intermediate of taxol. A key step involved a microwave-assisted alkylation reaction to construct the ABC ring system from an AC precursor. Subsequent formation of the D ring afforded baccatin III, a well-known precursor of taxol.

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Sigma-Aldrich
Baccatin III, ≥95% (HPLC)