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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 Enders✉(RWTH Aachen University)Klaus Breuer(RWTH Aachen University)J. Henrique Teles(BASF (United States))
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
Citations
216
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4.82
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Helvetica Chimica Acta · 1996 · 295 citations
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