4.8 Article

Direct and Metal-Catalyzed Photochemical Dimerization of the Phthalide (Z)-Ligustilide Leading to Both [2+2] and [4+2] Cycloadducts: Application to Total Syntheses of Tokinolides A-C and Riligustilide

Journal

ORGANIC LETTERS
Volume 21, Issue 16, Pages 6295-6299

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02172

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Funding

  1. Australian Research Council
  2. ANU Institute of Advanced Studies
  3. National Natural Science Fund of China [81872759]
  4. Pearl River Scholar Program of Guangdong Province

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Synthetically derived (Z)-ligustilide (1) has been subjected to photochemically-promoted dimerization processes under a range of conditions. By such means, varying distributions of the dimeric natural products tokinolides A-C (4, 3, and 6, respectively) and riligustilide (5) as well certain related (isomeric) compounds have been obtained. The structures of three of them have been confirmed by single-crystal X-ray analysis. The biosynthetic implications of the outcomes of this study are discussed.

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