The concept of internal solubilization in peptide synthesis: ethylene glycol-based protecting groups
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Synthesis of ‘difficult’ peptide sequences: application of a depsipeptide technique to the Jung–Redemann 10- and 26-mers and the amyloid peptide Aβ(1–42)
2. Improved preparation of amyloid-? peptides using DBU asN?-Fmoc deprotection reagent
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1. Synthesis of small protein domains by automated flow chemistry;Reaction Chemistry & Engineering;2024
2. The potential of N-alkoxymethyl groups as peptide backbone protectants;Tetrahedron Letters;2014-01
3. Recent trends in Cys- and Ser/Thr-based synthetic strategies for the elaboration of peptide constructs;Chemical Communications;2012
4. On the Synthesis of Conformationally Modified Peptides through Isonitrile Chemistry: Implications for Dealing with Polypeptide Aggregation;Journal of the American Chemical Society;2011-05-03
5. Orthogonal Protecting Groups and Side-Reactions in Fmoc/tBu Solid-Phase Peptide Synthesis;Amino Acids, Peptides and Proteins in Organic Chemistry;2011-01-31
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