The asymmetric synthesis of (−)-captopril utilising the iron chiral auxiliary [(η5-C5H5)Fe(CO)(PPh3)]
- 1 January 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (45) , 5563-5564
- https://doi.org/10.1016/s0040-4039(00)96782-0
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Improved stereochemical control and mechanistic aspects of the alkylation of enolates derived from [(η5-C5H5)Fe(CO)(PPh3)COCH2R]Tetrahedron Letters, 1986
- Conformational analysis and active site modeling of angiotensin-converting enzyme inhibitorsJournal of Medicinal Chemistry, 1985
- Chiral propionate enolate equivalents for the stereoselective synthesis of threo- or erytho-α,-methyl-β-hydroxy acidsTetrahedron Letters, 1985
- Stereoselective synthesis of erythro-β-hydroxy carboxylic acids via iron acyl complexesTetrahedron Letters, 1984
- An Improved Synthesis of CaptoprilJournal of Pharmaceutical Sciences, 1984
- The design and synthesis of new triazolo, pyrazolo-, and pyridazo-pyridazine derivatives as inhibitors of angiotensin converting enzymeJournal of the Chemical Society, Perkin Transactions 1, 1984
- Synthesis of captopril starting from an optically active .BETA.-hydroxy acid.CHEMICAL & PHARMACEUTICAL BULLETIN, 1982
- 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
- t-Butyl Esters of Amino Acids and Peptides and their Use in Peptide Synthesis1Journal of the American Chemical Society, 1960