2′-Amino-α-chloroacetophenone as a Valuable Tool for the Synthesis of Conveniently-Substituted α, β-Epoxychalcone Derivatives

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概要

• 論文の詳細を見る

• The synthesis of conveniently substituted 2′-amino-α, β-epoxychalcones is described. They were obtained through Darzens condensation of 2′-amino-3′, 5′-dimethoxy-α-chloroacetophenone with benzaldehydes. The latter can undergo different cyclization possibilities and afford a variety of flavonoid analogs with biological potential.

• 公益社団法人日本薬学会の論文
• 2005-04-01

著者

• Blanc Madeleine

  Department De Pharmacochimie Moleculaire Faculte De Pharmacie De Grenoble

• MARTIN Maud

  Department de Pharmacochimie Moleculaire, Faculte de Pharmacie de Grenoble

• OKOMBI Sabrina

  Department de Pharmacochimie Moleculaire, Faculte de Pharmacie de Grenoble

• BOUMENDJEL Ahcene

  Department de Pharmacochimie Moleculaire, Faculte de Pharmacie de Grenoble

• Boumendjel Ahcene

  Department De Pharmacochimie Moleculaire Faculte De Pharmacie De Grenoble

• Boumendjel Ahcene

  Departement De Pharmacochimie Moleculaire Umr-cnrs 5063 Universite Joseph Fourier De Grenoble Facult

• Martin Maud

  Department De Pharmacochimie Moleculaire Faculte De Pharmacie De Grenoble

• Okombi Sabrina

  Departement De Pharmacochimie Moleculaire Umr-cnrs 5063 Universite Joseph Fourier De Grenoble Facult

関連論文

• 2′-Amino-α-chloroacetophenone as a Valuable Tool for the Synthesis of Conveniently-Substituted α, β-Epoxychalcone Derivatives
• A One-Step Synthesis of 2-Alkyl-5-hydroxychromones and 3-Alkoyl-2-alkyl-5-hydroxychromones

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