[3] Cleavage methods following Boc-based solid-phase peptide synthesis
- 1 January 1997
- book chapter
- Published by Elsevier
- Vol. 289, 29-44
- https://doi.org/10.1016/s0076-6879(97)89042-8
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Two‐step hard acid deprotection/cleavage procedure for solid phase peptide synthesisInternational Journal of Peptide and Protein Research, 1991
- Mechanisms for the removal of benzyl protecting groups in synthetic peptides by trifluoromethanesulfonic acid-trifluoroacetic acid-dimethyl sulfideJournal of the American Chemical Society, 1986
- An SN2 deprotection of synthetic peptides with a low concentration of hydrofluoric acid in dimethyl sulfide: evidence and application in peptide synthesisJournal of the American Chemical Society, 1983
- Boron Tris(trifluoroacetate) for Removal of Protecting Groups in Peptide ChemistryAngewandte Chemie International Edition in English, 1973
- t-Amyloxycarbonyl as a New Protecting Group in Peptide Synthesis. IV. Synthesis and Use of t-Amyl AzidoformateBulletin of the Chemical Society of Japan, 1967