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Stereospecificity in radical carbon–carbon bond formation reactions based on tartaric acid
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1987
Year
Tartaric AcidAlkene MetathesisBiochemistryNatural SciencesRadical Decarboxylative AdditionRadical (Chemistry)Complete RetentionOrganic ChemistryStereoselective SynthesisChemistryProtected DerivativePharmacologyAsymmetric CatalysisEnantioselective Synthesis
Radical decarboxylative addition to activated alkenes, using the thiohydroxamic ester method, of a suitably protected derivative of (+)-L-tartaric acid leads to overall substitution of the carboxy group with essentially complete retention of configuration.