4.7 Article

Total Synthesis of Bulbophylol-B

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 71, Issue 11, Pages 1938-1941

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/np800226n

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Funding

  1. Shenyang Personnel Bureau
  2. Shenyang Science and Technology Bureau

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The first total synthesis of bulbophylol-B (1) has been achieved with the longest linear sequence of 12 steps and an overall yield of 17.9% via a new and practical approach to construct the dihydrodibenz[b,f]oxepin skeleton employing Wittig, selective reduction, and intramolecular Ullmann reactions as key steps.

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