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Four new diarylheptanoids from the roots of Juglans mandshurica

Gao Li1, Ming-Lu Xu, Han-Gon Choi

  • 1College of Pharmacy, Yeungnam University, Gyongsan, Korea.

Chemical & Pharmaceutical Bulletin
|March 4, 2003
PubMed

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The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.