Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Journal of Organic Chemistry called Manganese(III) Acetate Initiated Oxidative Free Radical Reactions between 2-Amino-1,4-naphthoquinones and β-Dicarbonyl Compounds, Author is Jiang, Ming-Chyuan; Chuang, Che-Ping, which mentions a compound: 18362-64-6, SMILESS is CC(C)C(CC(C(C)C)=O)=O, Molecular C9H16O2, Application In Synthesis of 2,6-Dimethyl-3,5-heptanedione.
Manganese(III) acetate oxidative free radical reaction between 2-amino-1,4-naphthoquinones and β-dicarbonyl compounds is described. With 2-anilino-1,4-naphthoquinone, benzo[b]acridine-6,11-dione and benzo[f]indole-4,9-diones were obtained. In most cases, benzo[b]acridine-6,11-dione is the major product. The reaction of 2-alkylamino-1,4-naphthoquinone with 1,3-diones gave benzo[f]indole as the only product. When 2-alkylamino-1,4-naphthoquinone was treated with β-keto esters, three benzo[f]indoles were obtained.
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Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica