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{N,N-Bis[2-(diphenyl-phosphan-yl)eth-yl]-aniline}(η-dibenzyl-ideneacetone)-palladium(0)

Seyma Gören Keskin1, Julie M Stanley, Michelle L Mejía

  • 1Department of Chemistry and Biochemistry, The University of Texas at Austin, 1 University Station, A5300, Austin, Texas 78712, USA.

Acta Crystallographica. Section E, Structure Reports Online
|November 9, 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.