131991-50-9Relevant articles and documents
Chiral Differentiation in the Deacylation of 6A-O-propanoyl>-β-cyclodextrin
Coates, John H.,Easton, Christopher J.,Eyk, Stephen J. van,May, Bruce L.,Singh, Paramjit,Lincoln, Stephen F.
, p. 759 - 760 (2007/10/02)
In 0.1 mol dm-3 sodium carbonate buffer at pH 11.5 the pseudo first-order rate constants for the hydrolysis of the diastereoisomers of the title compound to give Ibuprofen propanoic acid> and β-cyclodextrin are 2.97*10-5 s-1 and 3.16*10-4 s-1, with the diastereoisomer derived from (R)-Ibuprofen being the most susceptible to hydrolysis.