An acyliminium ion route to Cis and Trans “Anti” phe-gly dipeptide mimetics
- 31 December 1991
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 1 (6) , 309-312
- https://doi.org/10.1016/s0960-894x(01)80814-3
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- The conversion of a diazolactam to an α-methylenelactam: An entrance to new conformationally restricted inhibitors of angiotensin-converting enzymeTetrahedron Letters, 1990
- Interaction of Angiotensin I-Converting Enzyme with Two Potent Tricyclic InhibitorsJournal of Enzyme Inhibition, 1989
- An acyl-iminium ion cyclization route to a novel conformationally restricted dipeptide mimic: applications to angiotensin-converting enzyme inhibitionJournal of the American Chemical Society, 1987
- Mixed anhydrides in peptide synthesis. Influence of the solvent and the amine on the racemization of dmet residue of an enkephalin sequenceTetrahedron, 1987
- Racemisierungsfreie UmesterungN-geschützter Dipeptid-ester mit Hilfe von Titan(IV)-alkoxidenSynthesis, 1982
- Der 2‐Trimethylsilyläthyl‐Rest als selektiv abspaltbare Carboxy‐SchutzgruppeHelvetica Chimica Acta, 1977
- Synthesis of N-substituted aziridine-2-carboxylatesTetrahedron, 1977