Bifunctional chiral synthons via biochemical methods. VIII. Optically-active 3-aroylthio-2-methylpropionic acids.
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (43) , 5203-5206
- https://doi.org/10.1016/s0040-4039(00)85169-2
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Bifunctional chiral synthons via biochemical methods. : VII. Optically-active 2.2′-dihydroxy-1,1′-binaphthyl.Tetrahedron Letters, 1985
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982
- Synthesis of captopril starting from an optically active .BETA.-hydroxy acid.CHEMICAL & PHARMACEUTICAL BULLETIN, 1982
- Inhibition of the renin-angiotensin system. A new approach to the therapy of hypertensionJournal of Medicinal Chemistry, 1981
- Inhibitors of angiotensin-converting enzyme for treatment of hypertensionBiochemical Pharmacology, 1980
- Design of potent competitive inhibitors of angiotensin-converting enzyme. Carboxyalkanoyl and mercaptoalkanoyl amino acidsBiochemistry, 1977
- Design of Specific Inhibitors of Angiotensin-Converting Enzyme: New Class of Orally Active Antihypertensive AgentsScience, 1977