Stereoselective metabolism of 3-isopropyl-5-(1-naphthoxymethyl)oxazolidine, a prodrug of propranolol
Author:
Publisher
Elsevier BV
Subject
Pharmacology,Biochemistry
Reference17 articles.
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1. A Simple and Efficient Approach for the Synthesis of 1,3-Oxazolidines from β-Amino Alcohols Using Grinding Technique;ChemistrySelect;2018-12-21
2. New chemoenzymatic pathway for β-adrenergic blocking agents;Tetrahedron: Asymmetry;2005-04
3. Chemoenzymatic synthesis of (S) and (R)-propranolol and sotalol employing one-pot lipase resolution protocol;Bioorganic & Medicinal Chemistry Letters;2004-09
4. Synthesis, stereoselective enzymatic hydrolysis, and skin permeation of diastereomeric propranolol ester prodrugs;Journal of Pharmaceutical Sciences;1999-05
5. Stereoselective Hydrolysis of O‐Isovaleryl Propranolol and Its Influence on the Clearance of Propranolol after Oral Administration;Journal of Pharmaceutical Sciences;1994-12
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