Related Experiment Video
Updated: Jun 11, 2025

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs
Published on: January 17, 2020
Recent progress in asymmetric radical reactions enabled by chiral iron catalysts
1School of Pharmaceutical and Chemical Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China. jie_wu@fudan.edu.cn.
Abstract:
Transition-metal-catalyzed radical asymmetric reactions offer a versatile and effective platform for accessing chiral organic molecules with high enantiopurity. Given that iron is the most abundant and less toxic transition metalic element available, the application of iron catalysts is considered to be a more sustainable and attractive approach. Over the last decade, several exciting and notable achievements have been witnessed. In this highlight, we aim to provide an overview of the progress in ligand-enabled iron-catalyzed asymmetric radical reactions, with an emphasis on the reaction mechanisms.
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Radical Halogenation: Stereochemistry
Halogenation to form a new chiral center:
Radical Anti-Markovnikov Addition to Alkenes: Overview
Radical Reactivity: Concentration Effects
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Radical Reactivity: Steric Effects
Along with electronic...

