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Updated: Jan 25, 2026

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
Published on: May 28, 2014
Zirconium complexes supported by a ferrocene-based ligand as redox switches for hydroamination reactions
Yi Shen1, Scott M Shepard, Christopher J Reed
1Department of Chemistry & Biochemistry, University of California, Los Angeles, USA. pld@chem.ucla.edu.
Abstract:
The synthesis of (thiolfan*)Zr(NEt2)2 (thiolfan* = 1,1'-bis(2,4-di-tert-butyl-6-thiophenoxy)ferrocene) and its catalytic activity for intramolecular hydroamination are reported. In situ oxidation and reduction of the metal complex results in reactivity towards different substrates. The reduced form of (thiolfan*)Zr(NEt2)2 catalyzes hydroamination reactions of primary aminoalkenes, whereas the oxidized form catalyzes hydroamination reactions of secondary aminoalkenes.
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