4.7 Article

Synthesis and Structural Revision of Symbiodinolide C23-C34 Fragment

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 74, 期 13, 页码 4797-4803

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jo900546k

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资金

  1. Okayama Foundation for Science and Technology
  2. NOVARTIS Foundation (Japan
  3. The Mitsubishi Foundation
  4. Japan Society for the Promotion of Science [19710184, 21710231, 16GS0206]
  5. Grants-in-Aid for Scientific Research [19710184, 21710231] Funding Source: KAKEN

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Stereoselective synthesis of the C23-C34 fragment of symbiodinolide, which possesses the originally proposed stereochemistry, and its diastercomers was achieved in 19 steps from L-aspartic acid, respectively. Comparison of spectroscopic data of the synthetic products with those of the degraded product of symbiodinolide led to a structural revision of the C23-C34 fragment.

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