General synthesis of polyfunctionalized fluoromethyleneketone retroamides as potential inhibitors of thrombin
- 2 December 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (49) , 7255-7258
- https://doi.org/10.1016/0040-4039(91)80491-n
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Synthesis of peptidyl fluoromethyl ketones and peptidyl .alpha.-keto esters as inhibitors of porcine pancreatic elastase, human neutrophil elastase, and rat and human neutrophil cathepsin GJournal of Medicinal Chemistry, 1990
- New fluoroketones as human renin inhibitorsFEBS Letters, 1989
- X-ray diffraction analysis of the inhibition of porcine pancreatic elastase by a peptidyl trifluoromethylketoneJournal of Molecular Biology, 1988
- The α, α-Difluoro reformatsky reagent: Pregeneration and structural determinationJournal of Fluorine Chemistry, 1988
- Extended binding inhibitors of chymotrypsin that interact with leaving group subsites S1'-S3'Biochemistry, 1987
- Design and synthesis of potent and specific renin inhibitors containing difluorostatine, difluorostatone, and related analogsJournal of Medicinal Chemistry, 1986
- Thrombin specificityEuropean Journal of Biochemistry, 1985
- Organic sonochemistry. Sonic acceleration of the Reformatsky reactionThe Journal of Organic Chemistry, 1982
- Reformatsky reactions with o- and p-substituted benzophenonesCanadian Journal of Chemistry, 1968
- Reformatsky‐Reaktionen mit Substituierten BenzaldehydenEuropean Journal of Inorganic Chemistry, 1957