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Updated: May 30, 2026

Synthesis, Cellular Delivery and In vivo Application of Dendrimer-based pH Sensors
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Published on: September 10, 2013

催化色龙树状体的催化色龙树状体.

M Shema-Mizrachi1, G M Pavan, E Levin

  • 1Department of Chemistry, Ben-Gurion University, Beer-Sheva, Israel.

Journal of the American Chemical Society
|August 5, 2011
PubMed
概括

合成了具有可调节的乙烯末端的铁二烯树脂体. 改变末端组改变了它们的形状,并显著影响了各种基的催化环氧化活性和选择性.

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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.
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