An enantioselective synthesis of the C(33)- C(37) fragment of Amphotericin B

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Abstract

An enantioselective synthesis of the C(33)–C(37) tripropionate fragment of Amphotericin B has been developed in only 6 steps.

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Original languageEnglish
Pages (from-to)3193-3196
JournalORGANIC AND BIOMOLECULAR CHEMISTRY
Volume1
Issue number18
Publication statusPublished - 2003
MoE publication typeA1 Journal article-refereed

    Research areas

  • asymmetric synthesis, natural products, organic chemistry

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