facile and efficient conjugate additions of b-dicarbonyl compounds and nitroalkanes to 4-aryl-4-oxobut-2-enoates
Abstract
Facile and efficient conjugate additions of carbon nucleophiles, such as b-dicarbonyl compounds and nitroalkanes, to 4-aryl-4-oxobut-2-enoates have been achieved under simple base catalysis. A variety of multi-functional g-keto esters could be conveniently obtained in good to excellent yields with complete regioselectivity.
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