Simple synthesis of both enantiomers of the C7-C12 segment of epothilones

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Abstract

Both enantiomers of the C7-C12 segment (3 and 4) of antitumor antibiotics epothilones (1and 2) were synthesized from methyl (R)- and (S)-3-hydroxy-2-methylpropionate (5 and 6) in five steps in a fair yield. © 1998, Taylor & Francis Group, LLC. All rights reserved.

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Tanimori, S., Tanimoto, K., & Kirihata, M. (1998). Simple synthesis of both enantiomers of the C7-C12 segment of epothilones. Bioscience, Biotechnology and Biochemistry, 62(12), 2428–2430. https://doi.org/10.1271/bbb.62.2428

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