Synthesis of 3,5-disubstituted isoxazoles by domino reductive Nef reaction/cyclization of ß-nitroenones.

ß-Nitroenones can be efficiently converted into 3,5-disubstituted isoxazoles by using tin(II)chloride dihydrate and ethyl acetate as a reducing agent and solvent, respectively. Products are obtained in good yields and several functional groups are tolerated thanks to the mild reaction conditions.