Adams, Richard D. published the artcileSynthesis of 1,3-dioxolanes by addition of ketones to epoxides with [Cp*Ir(NCMe)3]2+ as catalyst, Related Products of dioxole, the publication is Journal of Organometallic Chemistry (1999), 582(2), 358-361, database is CAplus.
The title reactions proceeded readily at 22°, and the yields were good. The following 1,3-dioxolanes were prepared: 2,2,4-trimethyl-1,3-dioxolane, 2,2-dimethyl-4-vinyl-1,3-dioxolane, 2,2-dimethyl-4-phenyl-1,3-dioxolane, 2,2-diethyl-4-methyl-1,3-dioxolane, 2,2-diethyl-4-vinyl-1,3-dioxolane, 2,2-diethyl-4-phenyl-1,3-dioxolane. An inversion of configuration at the carbon atom at the C-O bond cleavage site of the epoxide was observed to occur in the formation of (R,S)-2,2,4,5-tetramethyl-1,3-dioxolane and a mixture of (R,R)- and (S,S)-2,2,4,5-tetramethyl-1,3-dioxolane from the reactions of acetone with (R,R)-/(S,S)-2-butene oxide and (R,S)-2-butene oxide, resp.
Journal of Organometallic Chemistry published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C6H12O2, Related Products of dioxole.
Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem