Convenient Synthesis and Physiological Activities of Flavonoids in Coreopsis lanceolata L. Petals and Their Related Compounds

Molecules. 2018 Jul 9;23(7):1671. doi: 10.3390/molecules23071671.

Abstract

Chalcones, flavanones, and flavonols, including 8-methoxybutin isolated from Coreopsis lanceolata L. petals, were successfully synthesized with total yields of 2⁻59% from O-methylpyrogallols using the Horner⁻Wadsworth⁻Emmons reaction as a key reaction. Aurones, including leptosidin, were also successfully synthesized with 5⁻36% total yields using the Aldol condensation reaction as a key reaction. Each chalcone, flavanone, flavonol, and aurone with the 3,4-dihydroxy groups in the B-ring showed high antioxidant activity. Additionally, each of the chalcones, flavanones, flavonols, and aurones with the 2,4-dihydroxy groups in the B-ring showed an excellent whitening ability.

Keywords: Coreopsis lanceolata L.; Horner–Wadsworth–Emmons reaction; aurone; chalcone; flavanone; flavonol.

MeSH terms

  • Antioxidants / chemical synthesis*
  • Antioxidants / chemistry
  • Antioxidants / pharmacology
  • Benzofurans / chemical synthesis
  • Benzofurans / chemistry
  • Benzofurans / pharmacology
  • Chalcone / chemical synthesis
  • Chalcone / chemistry
  • Chalcone / pharmacology
  • Coreopsis / chemistry*
  • Flavones / chemical synthesis
  • Flavones / chemistry
  • Flavones / pharmacology
  • Flavonoids / chemical synthesis*
  • Flavonoids / chemistry
  • Flavonoids / pharmacology
  • Flowers / chemistry
  • Molecular Structure
  • Plant Extracts / chemistry

Substances

  • Antioxidants
  • Benzofurans
  • Flavones
  • Flavonoids
  • Plant Extracts
  • aurone
  • Chalcone
  • flavone