Why do aromatic interactions matter of compound: 18362-64-6

Compounds in my other articles are similar to this one(2,6-Dimethyl-3,5-heptanedione)Electric Literature of C9H16O2, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Electric Literature of C9H16O2. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 2,6-Dimethyl-3,5-heptanedione, is researched, Molecular C9H16O2, CAS is 18362-64-6, about 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.

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.

Compounds in my other articles are similar to this one(2,6-Dimethyl-3,5-heptanedione)Electric Literature of C9H16O2, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica