Diels-Alder Reaction of in Situ Generated Quinones on a Lithium Perchlorate/Polyethyleneglycol Modified Electrode

  • Kazuhiro Chiba
  • Shokaku Kim
  • Masahiro Tada
Conference paper


Lithium perchlorate was highly concentrated on the polyethyleneglycol modified electrode and promoted Diels-Alder reactions. By using the modified electrode in acetonitrile, hydroquinones were efficiently oxidized to corresponding quinones which were immediately trapped by dienes to give varied cycloadducts.


Acrylic Acid Modify Electrode Cycloaddition Reaction Lithium Perchlorate Coated Electrode 
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Copyright information

© Springer Japan 1998

Authors and Affiliations

  • Kazuhiro Chiba
    • 1
  • Shokaku Kim
    • 1
  • Masahiro Tada
    • 1
  1. 1.Laboratory of Bio-organic ChemistryTokyo University of Agriculture and TechnologyFuchu, Tokyo 183Japan

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