First Total Synthesis of Amorfrutin C

  • ChemPubSoc Europe Logo
  • Author: ChemViews Magazine
  • Published Date: 25 January 2018
  • Source / Publisher: European Journal of Organic Chemistry/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
thumbnail image: First Total Synthesis of Amorfrutin C

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Amorfrutins are a family of natural products with a characteristic planar 2-hydroxybenzoic acid core. Some of these compounds are bioactive. Amorfrutin C (pictured), for example, was isolated from the roots of Glycyrrhiza foetida, a plant related to licorice. This natural product can inhibit human cancer cell proliferation.

Weijia Xie, China Pharmaceutical University, Nanjing, and colleagues have performed the first total syntheses of Amorfrutin C and the related compound pseudo-Amorfrutin A. The team started from commercially available 2,4,6-trihydroxybenzoic acid, which was converted to a protected 2,4-dihydroxybenzoic acid derivative. A prenyl moiety was introduced to this intermediate via a bromination reaction and a subsequent CuCN-meditated alkylation reaction. Using N-bromosuccinimide (NBS) to mediate the bromination led to the monoprenylated pseudo-Amorfrutin A. In contrast, using 1,3-dibromo-5,5-dimethylhydantoin (DBDMH) caused bromination at two positions of the central ring and led to the diprenylated Amorfrutin C.

The synthesis of Amorfrutin C was achieved with an overall yield of 16 % and that of pseudo-Amorfrutin A with a total yield of 29.3 %. According to the researchers, the results could be important for the further design and synthesis of Amorfrutin family derivatives in order to identify drug candidates.



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