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trans-Dichloridobis(4-methoxy-aniline-κN)palladium(II)

Volodimir Bon1, Svitlana Orysyk, Vasyl Pekhnyo

  • 1Institute of General and Inorganic Chemistry, NAS Ukraine, Kyiv, prosp. Palladina 32/34, 03680 Ukraine.

Acta Crystallographica. Section E, Structure Reports Online
|May 18, 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.