Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 2,6-Dimethyl-3,5-heptanedione, is researched, Molecular C9H16O2, CAS is 18362-64-6, about Palladium-catalyzed oxidative alkoxylation of α-alkenyl β-diketones to form functionalized furans.Related Products of 18362-64-6.
Treatment of 4-allyl-2,6-dimethyl-3,5-heptanedione (I) with a catalytic amount of PdCl2(CH3CN)2, and a stoichiometric amount of CuCl2, provided 3-isobutyryl-2-isopropyl-5-methylfuran (II) in good yield. A series of α-alkenyl β-diketones underwent oxidative alkoxylation, under these conditions, to give 2,3,5-trisubstituted furans in moderate to good yields.
Here is a brief introduction to this compound(18362-64-6)Related Products of 18362-64-6, if you want to know about other compounds related to this compound(18362-64-6), you can read my other articles.
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica