Related Experiment Video
Updated: Jul 14, 2026

Facile Preparation of 4-Substituted Quinazoline Derivatives
Published on: February 15, 2016
Probing the solvent-induced tautomerism of a redox-active ureidopyrimidinone
Anne-Marie Alexander1, Marc Bria, Gunther Brunklaus
1WestCHEM, Department of Chemistry, Joseph Black Building, University of Glasgow, Glasgow, UKG12 8QQ.
Abstract:
A ferrocene-functionalised ureidopyrimidinone has been synthesised that can signal the solvent-induced tautomerism of the dimeric 4[1H]-pyrimidinone form to the monomeric 6[1H]-pyrimidinone form.
More Related Videos
10:51The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
Published on: April 10, 2015
10:24Defining Hsp33's Redox-regulated Chaperone Activity and Mapping Conformational Changes on Hsp33 Using Hydrogen-deuterium Exchange Mass Spectrometry
Published on: June 7, 2018
Related Concept Videos
Redox Reactions
Redox Reactions
Redox Titration: Overview
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Redox Titration: Other Oxidizing and Reducing Agents