Fmoc-kompatible Festphasensynthese von langen, C-terminalen Peptidthioestern
- 17 September 2001
- journal article
- research article
- Published by Wiley in Angewandte Chemie
- Vol. 113 (18) , 3503-3505
- https://doi.org/10.1002/1521-3757(20010917)113:18<3503::aid-ange3503>3.0.co;2-u
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- 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
- Protein-Spleißen: Mechanismus und AnwendungenAngewandte Chemie, 2000
- Backbone Amide Linker (BAL) Strategy forNα-9-Fluorenylmethoxycarbonyl (Fmoc) Solid-Phase Synthesis of Unprotected Peptidep-Nitroanilides and Thioesters1The Journal of Organic Chemistry, 1999
- Lactone and Lactam Library Synthesis by Silver Ion-Assisted Orthogonal Cyclization of Unprotected PeptidesJournal of the American Chemical Society, 1999
- Polypeptide synthesis by the thioester methodBiopolymers, 1999
- Direct preparation of peptide thioesters using an Fmoc solid-phase methodTetrahedron Letters, 1998
- A novel method to synthesize cyclic peptidesTetrahedron Letters, 1998
- Chemoselective backbone cyclization of unprotected peptidesChemical Communications, 1997
- Unprotected Peptides as Building Blocks for the Synthesis of Peptide Dendrimers with Oxime, Hydrazone, and Thiazolidine LinkagesJournal of the American Chemical Society, 1995