Recommanded Product: 2,6-Dimethyl-3,5-heptanedione. 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 Palladium-Catalyzed Intramolecular Oxidative Alkylation of Unactivated Olefins. Author is Pei, Tao; Wang, Xiang; Widenhoefer, Ross A..
Reaction of 5,5-dimethyl-8-nonene-2,4-dione catalyzed by PdCl2(CH3CN)2 (5 mol %) in the presence of CuCl2 (2.5 equiv) at room temperature for 3 h formed 2-acetyl-3,6,6-trimethyl-2-cyclohexenone in 96% isolated yield. Palladium-catalyzed intramol. oxidative alkylation tolerated a range of substitution and was applicable to the synthesis of spirobicyclic compounds, e.g., I, and to the cyclization of ζ-alkenyl β-keto esters.
In some applications, this compound(18362-64-6)Recommanded Product: 2,6-Dimethyl-3,5-heptanedione is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica