Efficient methods for the synthesis of α-aminophosphonate fluoroalkyl esters
Author:
Funder
Wroclaw University of Technology Statute Funds
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Irreversible inhibition of serine proteases by peptide derivatives of (.alpha.-aminoalkyl)phosphonate diphenyl esters
2. Novel diphenyl esters of peptidyl α-aminoalkylphosphonates as inhibitors of chymotrypsin and subtilisin
3. Irreversible inhibition of serine proteases by peptidyl derivatives of α-aminoalkylphosphonate diphenyl esters
4. New potent cathepsin G phosphonate inhibitors
5. Peptide Length and Leaving-Group Sterics Influence Potency of Peptide Phosphonate Protease Inhibitors
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1. Three-component reaction between phenanthridine, acetylenic ketones and bis(polyfluoroalkyl) H-phosphonates: synthesis of E-N-acylethenyl-6-bis(polyfluoroalkyl)phosphoryl-5,6-dihydrophenanthridines;Russian Chemical Bulletin;2024-01
2. Synthesis of polyfluoroalkylphosphorylated dihydroquinolines and dihydroisoquinolines decorated with N-acylethenyl substituents by the reaction of bis(polyfluoroalkyl)phosphonates with electron-deficient acetylenes and quinolines;Journal of Fluorine Chemistry;2023-08
3. Reaction of polyfluoroalkyl dichlorophosphites with propargyl alcohol: synthesis and isomerization of polyfluoroalkyl di(2-propynyl) phosphites;Russian Chemical Bulletin;2021-11
4. Synthesis of Non-Symmetric Functionalized Polyfluoroalkyl Phosphites;Russian Journal of General Chemistry;2020-05
5. Catalyst- and Solvent-Free Synthesis of α-Amino Polyfluoroalkylphosphonates from Bis(fluoroalkyl) Phosphonates and Aldimines;Synthesis;2020-02-13
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