Synthesis and conformational studies of Zabicipril (S 9650-3), a potent inhibitor of angiotensin converting enzyme
- 1 November 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (48) , 7369-7372
- https://doi.org/10.1016/s0040-4039(00)60190-9
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Configuration and preferential solid-state conformations of perindoprilat (S-9780). Comparison with the crystal structures of other ACE inhibitors and conclusions related to structure-activity relationshipsJournal of Medicinal Chemistry, 1991
- Pharmacodynamic, pharmacokinetic and humoral effects of oral zabicipril, an angiotensin converting enzyme inhibitor in normotensive man.British Journal of Clinical Pharmacology, 1990
- SYNTHESIS OF [ S -( R ∗, R ∗)] – ETHYL α–[(1–CARBOXYETHYL) AMINO]–BENEZENEBUTANOATE, AN IMPORTANT INTERMEDIATE IN THE SYNTHESIS OF ANGIOTENSIN CONVERTING ENZYME INHIBITORSOrganic Preparations and Procedures International, 1983
- The reactions of 5-methoxyhydantoins with conjugated dienesTetrahedron, 1971
- Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1‐Hydroxy‐benzotriazolenEuropean Journal of Inorganic Chemistry, 1970