Issue 11, 1991

Chiral differentiation in the deacylation of 6A-O-{2-[4-(2-methylpropyl)phenyl]propanoyl}-β-cyclodextrin

Abstract

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 {2-[4-(2-methylpropyl)phenyl]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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 759-760

Chiral differentiation in the deacylation of 6A-O-{2-[4-(2-methylpropyl)phenyl]propanoyl}-β-cyclodextrin

J. H. Coates, C. J. Easton, S. J. van Eyk, B. L. May, P. Singh and S. F. Lincoln, J. Chem. Soc., Chem. Commun., 1991, 759 DOI: 10.1039/C39910000759

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements