A stereoconvergent strategy for the synthesis of enantiomerically pure (R)-(−) and (S)-(+)-2-(6-methoxy-2-naphthyl)-propanoic acid (naproxen)
- 1 January 1989
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 45 (13) , 4243-4252
- https://doi.org/10.1016/s0040-4020(01)81319-3
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Tartaric acid, an efficient chiral auxiliary: new asymmetric synthesis of 2-alkyl-2-arylacetic acidsThe Journal of Organic Chemistry, 1987
- Enantiomerically Pure 2-Bromoalkyl Aryl KetonesSynthesis, 1987
- Asymmetrische Bromierung enantiomerenreiner Acetale von AlkylarylketonenAngewandte Chemie, 1986
- Asymmetric Bromination of Enantiomerically Pure Acetals of Alkyl Aryl KetonesAngewandte Chemie International Edition in English, 1986
- Enantiomeric Purity of Naproxen by Liquid Chromatographic Analysis of Its Diastereomeric Octyl EstersJournal of Pharmaceutical Sciences, 1979
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- Nonsteroidal antiinflammatory agents. I. 6-Substituted 2-naphthylacetic acidsJournal of Medicinal Chemistry, 1970