Helvetica Chimica Acta · 1988 · 36 citations · 10 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsAmino Acid ChemistryEnzyme InhibitionAmino Acid StereochemistryChiral Resolution Of Amino AcidsEnantioselective SynthesisEnzyme Inhibitor DiscoveryEnzyme Inhibitor Synthesis
Note on the Synthesis of an Optically Active ACE Inhibitor with Amino‐oxo‐benzazepine‐1‐alkanoic‐Acid Structure by Means of an Enantioconvergent Crystallization‐Based Resolution An enantioselective synthesis of the potent angiotensin‐converting enzyme inhibitor (1′ S ,3 S )‐3‐[(1′‐(ethoxy‐carbonyl)‐3′‐phenylpropyl)amino]‐2,3,4,5‐tetrahydro‐2‐oxo‐1 H ‐1‐benzazepine‐1‐acetic acid hydrochloride ( 3 ) is described which user a crystallization‐based resolution of a racemic amino intermediate with concomitant racemization of the unwanted enantiomer.
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A new class of angiotensin-converting enzyme inhibitors
Arthur A. Patchett, Elbert E. Harris, Edward W. Tristram et al. · Nature · 1980 · 706 citations
Jeffrey W. H. Watthey, James L. Stanton, Mahesh Desai et al. · Journal of Medicinal Chemistry · 1985 · 127 citations · Full text