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2,2'-Bis(4-methoxy-phen-yl)-2,2'-bis-(tri-methyl-silan-yloxy)-2,2'-(ferrocene-1,1'-diyl)diacetonitrile

Xiao-Li Wang1, Huaying Bao

  • 1College of Chemistry, Beijing Normal University, Beijing 100875, People's Republic of China.

Acta Crystallographica. Section E, Structure Reports Online
|January 5, 2011
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.