Synthesis of P1 aspartate-based peptide acyloxymethyl and fluoromethyl ketones as inhibitors of interleukin-1β-converting enzyme
- 26 December 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (52) , 9693-9696
- https://doi.org/10.1016/0040-4039(94)88361-0
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Crystal structure of the cysteine protease interleukin-1β-converting enzyme: A (p20/p10)2 homodimerCell, 1994
- Structure and mechanism of interleukin-lβ converting enzymeNature, 1994
- P1 Aspartate-Based Peptide .alpha.-((2,6-Dichlorobenzoyl)oxy)methyl Ketones as Potent Time-Dependent Inhibitors of Interleukin-1.beta.-Converting EnzymeJournal of Medicinal Chemistry, 1994
- An improved procedure for the preparation of the Dess-Martin periodinaneThe Journal of Organic Chemistry, 1993
- New inhibitors of cysteine proteinases. Peptidyl acyloxymethyl ketones and the quiescent nucleofuge strategyJournal of the American Chemical Society, 1988
- A versatile synthesis of peptidyl fluoromethyl ketonesTetrahedron Letters, 1986
- Synthesis of peptide fluoromethyl ketones and the inhibition of human cathepsin BAnalytical Biochemistry, 1985
- Enantioselective synthesis of (R)- and (S)-4-[(methoxycarbonyl)-methyl]-2-azetidinones from D-glyceraldehyde acetonideTetrahedron Letters, 1983