REACTION OF SULFOXIMIDES WITH DIAZOMALONATE IN THE PRESENCE OF CU-SALT - NEW SYNTHESIS AND STEREOCHEMISTRY OF OPTICALLY-ACTIVE OXOSULFONIUM YLIDES

Sulphoximides (Ia-Ie) were found to react with dimethyl diazomalonate (DDM) in the presence of a catalytic amount of Cu-salts affording the corresponding oxosulphonium ylides in moderate yields. The reaction did not proceed at all under irradiation of UV light. (-)-Methylphenyloxosulphonium bis(methoxycarbonyl)-methylide ((-)-IIb) was obtained from (+)-(S)-methylphenylsulphoximide ((+)-(S)-Ib) together with (-)-(S)-methyl phenyl sulphoxide ((-)-(S)-IIIb) by this reaction. Hydrolysis of (-)-IIb gave (+)-methylphenyloxosulphonium methoxycarbonylmethylide ((+)-IIf) which was converted to (-)-(S)-IIIb upon treatment with dibenzoylethylene. Stereochemical cycle starting from (+)-(S)-Ib to (-)-(S)-IIIb was established and the absolute configurations of both ylides, (-)-IIb and (+)-IIf were assigned as (R)-configuration. The stereochemical courses, namely from (+)-(S)-Ib or (-)-(S)-IIIb to (-)-(R)-IIb or (+)-(R)-IIf to (-)-(S)-IIIb were determined as retention processes. The optical purities of the oxosulphonium ylides obtained from both reactions, (+)-(S)-Ib→(-)-(R)-IIb and (-)-(S)-IIIb→(-)-(R)-IIb, were almost equal. These results indicate that the mechanism of the reaction of sulphoximides with carbenes (or carbenoids) involves the initial formation of the sulphoxides which react subsequently with carbenes to afford the final products. © 1979.