Abstract
A manganese(III)-mediated oxidative free radical cyclization of 2-(ethoxycarbonylmethyl)-1,4-naphthoquinone
derivatives is described. These starting 2-(ethoxycarbonylmethyl)-1,4-naphthoquinones
can be synthesized effectively from the reaction of corresponding 1,4-naphthoquinones
with ethyl nitroacetate. With 2-benzyl-3-(ethoxycarbonylmethyl)-1,4-naphthoquinones,
naphthacene-5,12-diones were produced effectively in high selectivity. With ethyl
2-benzoyl-3-(ethoxycarbonylmethyl)-1,4-naphthoquinones, in addition to the expected
6-hydroxynaphthacene-5,12-diones, the novel naphtho[2,3-c]furan-4,9-diones were also formed as the major product.
Key words
manganese(III) acetate - oxidative - free radical - cyclization - 2-(ethoxycarbonylmethyl)-1,4-naphthoquinones