One-Pot Synthesis of Highly Conjugated Benzofuran Derivatives Based on Electrochemical Oxidation of Benzenediols in the Presence of Dibenzoylmethane

スポンサーリンク

概要

• 論文の詳細を見る

• Electrochemical oxidation of benzenediols (1-4) has been studied in the presence of dibenzoylmethane (5) as a nucleophile using cyclic voltammetry and controlled-potential coulometry. The results indicate that the electrochemically generated quinones participate in Michael addition reaction with 5 via various mechanisms to produce new benzofuran derivatives. We derived various products based on electrochemical oxidation in the controlled potential condition, at carbon electrode without toxic reagents in an undivided cell and ambient condition.

• 公益社団法人日本薬学会の論文
• 2007-06-01

著者

• NEMATOLLAHI Davood

  Faculty of Chemistry, Bu-Ali Sina University

• Nematollahi Davood

  Faculty Of Chemistry Bu-ali Sina University

• RAFIEE Mohammad

  Faculty of Chemistry, Bu-Ali Sina University

• Rafiee Mohammad

  Faculty Of Chemistry Bu-ali Sina University

関連論文

• An Environmentally Friendly Electrochemical Method for Synthesis of Benzofuranoquinone Derivatives
• Mechanistic Study of Electrochemical Oxidation of 2,5-Dihydroxybenzoic Acid and 3,4-Dihydroxybenzaldehyde in the Presence of 3-Hydroxy-1H-phenalene-1-one
• Electrochemical Synthesis of 4-(Dihydroxyphenylthio)-2H-chromen-2-one Derivatives
• One-Pot Synthesis of Highly Conjugated Benzofuran Derivatives Based on Electrochemical Oxidation of Benzenediols in the Presence of Dibenzoylmethane
• Electrochemical Oxidation of 4-Methylcatechol in the Presence of β-Diketones
• Catecholthioether Derivatives: Preliminary Study of in-Vitro Antimicrobial and Antioxidant Activities

スポンサーリンク