Solid-Phase Synthesis of C-Terminus Cysteine Peptide Acids
- 15 November 2022
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Process Research & Development
- Vol. 26 (12) , 3323-3335
Abstract
No abstract availableKeywords
Funding Information
- South African Agency for Science and Technology Advancement (120386)
This publication has 52 references indexed in Scilit:
- 4-Methoxybenzyloxymethyl Group, a Racemization-Resistant Protecting Group for Cysteine in Fmoc Solid Phase Peptide SynthesisOrganic Letters, 2012
- Cysteine Function Governs Its Conservation and Degeneration and Restricts Its Utilization on Protein SurfacesJournal of Molecular Biology, 2010
- Preparation and Use of Cysteine Orthoesters for Solid-Supported Synthesis of PeptidesOrganic Letters, 2010
- NovelS-Xanthenyl Protecting Groups for Cysteine and Their Applications for theNα-9-Fluorenylmethyloxycarbonyl (Fmoc) Strategy of Peptide Synthesis1-3The Journal of Organic Chemistry, 1997
- Synthesis of the very acid‐sensitive Fmoc‐Cys(Mmt)‐OH and its application in solid‐phase peptide synthesisInternational Journal of Peptide and Protein Research, 1996
- S-Phenylacetamidomethyl (Phacm): an orthogonal cysteine protecting group for Boc and Fmoc solid-phase peptide synthesis strategiesJournal of the Chemical Society, Perkin Transactions 1, 1995
- Racemization studies in peptide chemistry. Re-investigation of the “β-elimination–readdition” mechanism of N-benzyloxycarbonyl-S-benzylcysteine derivativesChemical Communications (London), 1968
- Racemization in peptide synthesis. Mechanism-specific modelsChemical Communications (London), 1967
- Solid Phase Peptide Synthesis. I. The Synthesis of a TetrapeptideJournal of the American Chemical Society, 1963
- N-Tritylamino Acids and Peptides. A New Method of Peptide Synthesis1Journal of the American Chemical Society, 1956