JOURNAL of the Tunisian Chemical Society

serving the Research, the Education and the Industry

Highly stereoselective synthesis of some β-branched α-(phenylsulfonylmethyl) acrylic compounds

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Substitution reaction of E-branched Baylis-Hillman bromides with sodium benzenesulfinate in absolute ethanol at room temperature, produces in SN2 process and high stereoselectivity, the corresponding allyl phenyl sulfinates in good yields.

S. Khamri, T. Turki, H. Amri

Baylis-Hillman derivatives, nucleophilic substitution, allyl phenyl sulfones

Pages 149-155

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