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A Novel Asymmetric Benzoin Reaction Catalyzed by a Chiral Triazolium Salt. Preliminary communication

Helvetica Chimica Acta · 1996 · Vol. 79(4) · pp. 1217–1221
Dieter EndersKlaus BreuerJ. Henrique Teles

Abstract

Abstract Using the chiral triazolium salt 1 as catalyst, a novel asymmetric variant of the benzoin reaction is reported. For the first time, the scope of the method is extended to a broader range of aromatic aldehydes 2 , affording the acyloins 3a–h in yields of 22–72% and enantiomeric excesses up to 86%.

N-Heterocyclic Carbenes in Organic and Inorganic ChemistryCoordination Chemistry and OrganometallicsSynthetic Organic Chemistry MethodsChemistryBenzoinEnantiomerScope (computer science)Salt (chemistry)CatalysisEnantioselective synthesisEnantiomeric excessOrganic chemistryCombinatorial chemistry
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N‐Heterocyclic Carbenes
Angewandte Chemie International Edition in English · 1997 · 1,675 citations
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