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Bicarbonate-binding catalysis for the enantioselective desymmetrization of keto sulfonium salts
José Alemán1,2,3, Jorge Humbrías-Martín4, Roberto Del Río-Rodríguez4
1Departamento de Química Orgánica (módulo 1), Universidad Autónoma de Madrid, Cantoblanco, Madrid, Spain. jose.aleman@uam.es.
Abstract:
Herein, an enantioselective desymmetrization of cyclic keto sulfonium salts through enantioselective deprotonation/ring opening process by anion-binding catalysis is presented. We report a squaramide/HCO3- complex as catalytic active species which is able to stereo-differentiate two enantiomeric protons, triggering the ring opening event taking advantage of the great tendency of sulfonium salts to act as leaving groups. Thus, this desymmetrization methodology give rise to β-methylsulfenylated sulfa-Michael addition type products with excellent yields and very good enantioselectivities. The bifunctional organocatalyst has been demonstrated to be capable of activating simultaneously the base and the keto sulfonium salt by DFT calculations and experimental proofs.
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