A Stereoselective Synthesis of N-[(S)-1-Ethoxycarbonyl-3-phenylpropyl]-l-alanine Derivatives by Means of Reductive Amination
- 5 October 1988
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 17 (10) , 1691-1694
- https://doi.org/10.1246/cl.1988.1691
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Synthesis of N2-[(S)-1-Carboxy-3-phenylpropyl]-L-lysyl-L-proline (Lisinopril)Journal of Pharmaceutical Sciences, 1985
- Reductive amination of ethyl 2-oxo-4-phenylbutanoate with L-alanyl-L-proline. Synthesis of enalapril maleateThe Journal of Organic Chemistry, 1984
- A favourable diastereoselective synthesis of N-(1-S-ethoxycarbonyl-3-phenylpropyl)-S-alanineTetrahedron Letters, 1984
- A General, One-Step Synthesis of α-Keto EstersSynthetic Communications, 1981
- A new class of angiotensin-converting enzyme inhibitorsNature, 1980
- Design of Specific Inhibitors of Angiotensin-Converting Enzyme: New Class of Orally Active Antihypertensive AgentsScience, 1977
- 1,3,2-Benzodioxaborole, a convenient monofunctional hydroborating agent. Simple new synthesis of alkaneboronic esters and acids from olefins via hydroborationJournal of the American Chemical Society, 1971