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A fourth-generation carbazole-phenylazomethine dendrimer as a size-selective host for fullerenes

Ken Albrecht1, Yuto Kasai, Yasunori Kuramoto

  • 1Chemical Resources Laboratory, Tokyo Institute of Technology, 4259 Nagatsuta, Yokohama 226-8503, Japan.

Chemical Communications (Cambridge, England)
|October 31, 2012
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.