Preparation of Useful Synthetic Intermediates of Taxol Analogs, Cyclooctenone Derivatives.

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  • Preparation of Useful Synthetic Interme

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Abstract

Stereoselective syntheses of ω-(α-bromoketo) octanals and nonanal with oxygenated functions and formation of the corresponding eight-membered carbocyclic aldols by subsequent samarium(II)-mediated cyclization are demonstrated. Cyclooctenones deoxygenated at the C2 or C10 position in the taxane framework are prepared by dehydration of the above aldols.

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