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Synthesis of highly fluorescent y-enyne dendrimers with four and six arms

Bilal R Kaafarani1, Brigitte Wex, Fei Wang

  • 1Center for Photochemical Sciences, Bowling Green State University, Bowling Green, Ohio 43403, USA.

The Journal of Organic Chemistry
|June 21, 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.