Related Experiment Video

Updated: Jun 1, 2026

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
07:07

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology

Published on: March 12, 2015

Supramolecular Nanocycles Comprising β-Cyclodextrin-click-Ferrocene Units: Rings of Rings of Rings

Maricica Munteanu1, Ute Kolb, Helmut Ritter

  • 1Institut für Organische Chemie und Makromolekulare Chemie, Heinrich-Heine Universität, Universitätsstrasse 1, 40225 Düsseldorf, Germany.

Macromolecular Rapid Communications
|May 19, 2011
PubMed

More Related Videos

Design, Synthesis, and Photochemical Properties of Clickable Caged Compounds09:44

Design, Synthesis, and Photochemical Properties of Clickable Caged Compounds

Published on: October 15, 2019

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules08:40

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules

Published on: April 28, 2014

Related Concept Videos

[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction01:16

[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

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.