4.8 Article

Discovery of Presaccharothriolide X, a Retro-Michael Reaction Product of Saccharothriolide B, from the Rare Actinomycete Saccharothrix sp A1506

Journal

ORGANIC LETTERS
Volume 20, Issue 15, Pages 4406-4410

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b01535

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Funding

  1. MEXT, Japan [17H06401, 26102726, 17K19233]
  2. AMED, Japan

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The highly reactive precursor molecule, presaccharothriolide X, was successfully isolated from the rare actinomycete Saccharothrix sp. A1506. The comparable biological activity of presaccharothriolide X and its Michael addition product saccharothriolide B unveils a unique masking/activating property of 2-aminophenol. Unexpectedly, 2-aminophenol in saccharothriolide B was eliminated through a retro-Michael reaction, to yield presaccharothriolide X under physiological conditions. 2-Aminophenol might be developed into a useful protecting group for bioactive small molecules with an alpha,beta-unsaturated ketone.

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