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Updated: Aug 23, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Nucleophilic carbenes in asymmetric organocatalysis
Dieter Enders1, Tim Balensiefer
1Institute of Organic Chemistry, Technical University of Aachen, Professor-Pirlet-Strasse 1, 52074 Aachen, Germany. enders@rwth-aachen.de
Abstract:
The coenzyme thiamine (vitamin B1), a natural thiazolium salt, is involved in many enzymatic catalyses. Since it has been proposed that the catalytically active species of these reactions is a nucleophilic carbene, many chemists have tried to perform enzyme mimetic asymmetric carbene catalysis. After a long and difficult search, stable carbenes are finally isolated, characterized, and in the chemist's hands. The experiments of decades have finally resulted in successful enantioselective benzoin condensations and enantioselective intramolecular Stetter reactions as important examples of carbene catalyzed asymmetric nucleophilic acylation processes.
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