Total synthesis of the antitumor antibiotic (+/-)-fredericamycin A by a linear approach |
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Authors: | Kita Y Iio K Kawaguchi K Fukuda N Takeda Y Ueno H Okunaka R Higuchi K Tsujino T Fujioka H Akai S |
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Affiliation: | Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Japan. kita@phs.osaka-u.ac.jp |
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Abstract: | A linear approach to the total synthesis of racemic fredericamycin A (1) through the oxidative intramolecular [4 + 2] cycloaddition of a (phenylthio)acetylene-cobalt complex is described, which is applicable for the asymmetric total synthesis of naturally occuring 1. The highlight of this work is the aromatic Pummerer-type reaction with 1-ethoxyvinyl chloroacetate, which effects the introduction of the oxygen functional group to the internal B-ring of the highly functionalized, congested polyaromatic ABC-ring moiety. |
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