Practical synthesis of hydroxychromenes and evaluation of their biological activity

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Abstract

A simple and efficient seven steps synthesis of brodifacoum and difethialone from phenylacetyl chloride is described. The key synthetic strategies involve Friedel-Crafts acylation, intramolecular ring cyclization and condensation reaction in the presence of Brønsted-Lowry acids. It was found that brodifacoum showed favorable inhibiting activities on LPS-stimulated nitrite production in BV-2 microglia cells. Brodifacoum exhibited superior anti-inflammatory effects than difethialone. We expect that an efficient linear synthesis of 4-hydroxycoumarin derivatives and key fragments that are useful agents for the modulation of inflammation as well as inhibition of coagulation will be of practical use. © 2012 by the authors.

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Jung, J. C., & Oh, S. (2012). Practical synthesis of hydroxychromenes and evaluation of their biological activity. Molecules, 17(1), 240–247. https://doi.org/10.3390/molecules17010240

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