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The Catalytic Asymmetric Michael Reaction of Tin(II) Enethiolates
35
Citations
5
References
1988
Year
Chemical EngineeringEngineeringCatalytic AmountsOrganic ChemistryStannous TriflateCatalysisStereoselective SynthesisChemistryOrganometallic CatalysisAsymmetric CatalysisEnantioselective SynthesisChiral Diamine
Abstract The catalytic asymmetric Michael reaction of tin(II) enethiolates forming 5-oxodithioesters in high yield with moderate to good enantioselectivity is achieved by employing catalytic amounts of stannous triflate and chiral diamine.
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