Published September 30, 1970
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Alkylation of β-Ketosulphoxides with Electrophillic Olefins
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β-ketosulphoxides undergo facile Michael reaction with \(\alpha\),β-unsaturated esters, ketones and nitriles. Reductive cleavage of the C-S bond, in the Michael reaction products so obtained, with aluminium amalgam in aq. T.H.F. provides a series of attractive multifunctional organic compounds.
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