Prodrugs as Drug Delivery Systems XXV: Hydrolysis of Oxazolidines—A Potential New Prodrug Type

This publication has 14 references indexed in Scilit:

• Pro-drugs as drug delivery systems XXI. Preparation, physicochemical properties and bioavailability of a novel water-soluble pro-drug type for carbamazepine☆
  International Journal of Pharmaceutics, 1982
• Enol esters as potential prodrugs. IV. Enhanced delivery of the quaternary species coralyne to rat brain using 6′-acetylpapaverin and its enol esters as prodrugs☆
  International Journal of Pharmaceutics, 1982
• Pro-drugs as drug delivery systems XX. Oxazolidines as potential pro-drug types for β-aminoalcohols, aldehydes or ketones
  International Journal of Pharmaceutics, 1982
• Enol esters as potential pro-drugs II. In vitro aqueous stability and enzyme-mediated hydrolysis of several enol esters of acetophenone
  International Journal of Pharmaceutics, 1981
• Pro-drugs as drug delivery systems VIII. Bioreversible derivatization of hydantoins by N-hydroxymethylation
  International Journal of Pharmaceutics, 1980
• Degradation of (—)-ephedrine in solution and during extraction with diethyl ether
  Journal of Pharmacy and Pharmacology, 1978
• Rationale for Design of Biologically Reversible Drug Derivatives: Prodrugs
  Journal of Pharmaceutical Sciences, 1975
• Kinetics of the dehydration of methylene glycol in aqueous solution
  Proceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences, 1966
• Nuclear Magnetic Resonance Spectra and Configuration. The N.m.r. Spectra of Diastereoisomeric Heterocyclic Derivatives of the Ephedrines
  Journal of the American Chemical Society, 1959
• Untersuchungen zum Konstellationsproblem in der Ephedrinreihe
  European Journal of Organic Chemistry, 1958