Peptide αthioester formation using standard Fmoc-chemistry
- 1 April 2003
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 44 (17) , 3551-3554
- https://doi.org/10.1016/s0040-4039(03)00582-3
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Recent advances in the application of expressed protein ligation to protein engineeringCurrent Opinion in Biotechnology, 2002
- An improved deblocking agent for direct Fmoc solid-phase synthesis of peptide thioestersTetrahedron Letters, 2002
- Synthesis of Native Proteins by Chemical LigationAnnual Review of Biochemistry, 2000
- Dissecting the Chemistry of Protein Splicing and Its ApplicationsAngewandte Chemie International Edition in English, 2000
- Fmoc-Based Synthesis of Peptide-αThioesters: Application to the Total Chemical Synthesis of a Glycoprotein by Native Chemical LigationJournal of the American Chemical Society, 1999
- Solid Phase Synthesis of Peptide C-Terminal Thioesters by Fmoc/t-Bu ChemistryJournal of the American Chemical Society, 1999
- Backbone Amide Linker (BAL) Strategy forNα-9-Fluorenylmethoxycarbonyl (Fmoc) Solid-Phase Synthesis of Unprotected Peptidep-Nitroanilides and Thioesters1The Journal of Organic Chemistry, 1999
- Direct preparation of peptide thioesters using an Fmoc solid-phase methodTetrahedron Letters, 1998
- Preparation of Peptide Thioesters using Fmoc-Solid-Phase Peptide Synthesis and its Application to the Construction of a Template-Assembled Synthetic Protein (TASP)Tetrahedron Letters, 1997
- Synthesis of Proteins by Native Chemical LigationScience, 1994