Bennet, Andrew J. published the artcileOxygen-18 and secondary deuterium kinetic isotope effects confirm the existence of two pathways for acid-catalyzed hydrolyses of α-arabinofuranosides, Safety of 2,2,4-Trimethyl-1,3-dioxolane, the publication is Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) (1985), 1233-6, database is CAplus.
The 18O kinetic isotope effects observed in the HClO4-catalyzed hydrolysis of 4-nitrophenyl and iso-Pr α-arabinofuranoside-1–18O and the secondary D effect observed in the hydrolysis of propan-2-yl-2–d α-arabinofuranoside suggest that the nitrophenyl glycoside reacts with exocyclic C-O cleavage and the propan-2-yl glycoside by endocyclic C-O cleavage.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999) 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, Safety of 2,2,4-Trimethyl-1,3-dioxolane.
Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem