Solid phase synthesis of aminoboronic acids: potent inhibitors of the hepatitis C virus NS3 proteinase
- 27 July 2000
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 10 (14) , 1577-1579
- https://doi.org/10.1016/s0960-894x(00)00284-5
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Boronic ester as a linker system for solid phase synthesisTetrahedron Letters, 1999
- The Design and Synthesis of Potent Inhibitors of Hepatitis C Virus NS3–4A ProteinaseAntiviral Chemistry and Chemotherapy, 1999
- Hepatitis C virus NS3/4A proteaseCurrent Opinion in Infectious Diseases, 1997
- Design of a novel class of bifunctional thrombin inhibitors, synthesised by the first application of peptide boronates in solid phase chemistryTetrahedron Letters, 1997
- Synthetic Inhibitors of ElastaseMedicinal Research Reviews, 1994
- .alpha.-Halo boronic esters: intermediates for stereodirected synthesisChemical Reviews, 1989