Tandem catalytic oxidative deacetylation of acetoacetic esters and heteroaromatic cyclizations.

One pot syntheses of furan, thiophene, and pyrrole were accomplished by oxidative deacetylation using Mn(III)/Co(II) catalysts and the Paal-Knorr reaction from 1,5-dicarbonyl compounds, which are prepared from the conjugate addition of ethyl acetoacetate to α,ß-unsaturated carbonyl compounds. The oxidative deacetylation and reductive cyclization of ß-ketoesters derived from ethyl acetoacetate and o-nitrobenzyl bromides efficiently produced diversely substituted indoles.