Deprotection Strategies for Thioimidates during Fmoc Solid-Phase Peptide Synthesis: A Safe Route to Thioamides
Author:
Affiliation:
1. Department of Chemistry, Iowa State University, Ames, Iowa 50011, United States
Funder
Division of Chemistry
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02317
Reference35 articles.
1. An Evaluation of Peptide-Bond Isosteres
2. Biosynthesis and Chemical Applications of Thioamides
3. Conformational Stability of Helical Peptides Containing a Thioamide Linkage
4. Thioamides in the collagen triple helix
5. The effects of thioamide backbone substitution on protein stability: a study in α-helical, β-sheet, and polyproline II helical contexts
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1. Thioimidate Solutions to Thioamide Problems during Thionopeptide Deprotection;Organic Letters;2024-02-11
2. Thioimidates provide general access to thioamide, amidine, and imidazolone peptide-bond isosteres;Methods in Enzymology;2024
3. Contemporary Applications of Thioamides and Methods for their Synthesis;Chemistry – A European Journal;2023-12-21
4. Thioamide Analogues of MHC I Antigen Peptides;Journal of the American Chemical Society;2023-11-15
5. A General Strategy to Install Amidine Functional Groups Along the Peptide Backbone;Journal of the American Chemical Society;2022-12-05
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