4.8 Article

Total Synthesis of Polygalolide A

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ORGANIC LETTERS
卷 13, 期 24, 页码 6532-6535

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AMER CHEMICAL SOC
DOI: 10.1021/ol2028256

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  1. Japan Society for the Promotion of Science (JSPS)
  2. Suntory Institute for Bioorganic Research
  3. Daiko Foundation
  4. Nagoya University
  5. Grants-in-Aid for Scientific Research [20380067, 22780102] Funding Source: KAKEN

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The total synthesis of polygalolide A was accomplished through intramolecular C-glycosylation of glucal modified with siloxyfuran. The siloxyfuran group and siloxy substituent at the C-3 position played crucial roles in allowing direct access to the highly substituted oxabicyclo[3.2.1] core skeleton with correct quaternary stereogenic centers.

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