Related Experiment Video
Updated: Jun 1, 2026

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)
Published on: January 17, 2020
Chiral Brønsted acids in enantioselective carbonyl activations--activation modes and applications
Magnus Rueping1, Alexander Kuenkel, Iuliana Atodiresei
1Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany. Magnus.Rueping@rwth-aachen.de
Abstract:
Chiral phosphoric acids and derivatives have attracted considerable attention as a powerful tool in asymmetric catalysis. Various enantioselective reactions have been developed by using these efficient Brønsted acid organocatalysts. Although initially the activation was restricted to reactive Brønsted basic substrates, recent reports are demonstrating the versatility of phosphoric acid catalysts in the activation of carbonyl compounds in a stereochemically controlled fashion. This tutorial review gives an overview of enantioselective Brønsted acid catalyzed transformations with the main focus on carbonyl activation. Different activation modes, key features of the catalysts and the applied substrates are presented and discussed with the goal to elucidate the origin of stereoselectivity in these Brønsted acid catalyzed transformations.
More Related Videos
07:36Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
06:31Highly Stereoselective Synthesis of 1,6-Ketoesters Mediated by Ionic Liquids: A Three-component Reaction Enabling Rapid Access to a New Class of Low Molecular Weight Gelators
Published on: November 27, 2015
Related Concept Videos
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Prochirality
Stereochemical Effects of Enolization
Radical Anti-Markovnikov Addition to Alkenes: Overview
α-Alkylation of Ketones via Enolate Ions
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction