4.8 Article

Biomimetic Total Syntheses of Sanctis A-B with Structure Revision

Journal

ORGANIC LETTERS
Volume 22, Issue 3, Pages 934-938

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b04486

Keywords

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Funding

  1. National Natural Science Foundation of China [81773602]
  2. Natural Science Foundation of Guangdong Province [2019A1515011694]
  3. Pearl River Science and Technology New Star Fund of Guangzhou [201605120849569]
  4. Guangdong Special Support Program [2017TQ04R599]

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The first concise total syntheses of sanctis A and B were reported, and it enabled revision of the structure of sanctis B through single-crystal X-ray diffraction. The established synthetic approach mainly mimics a biosynthetic olefin isomerization/hemiacetalization/dehydration/[3 + 3]-type cycloaddition cascade sequence, offering a viable synthetic methodology to efficiently access sanctis A-B and their analogues.

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