Preparation of peptide thioesters using Fmoc strategy through hydroxyl side chain anchoring
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference34 articles.
1. Synthesis of Proteins by Native Chemical Ligation
2. Solid Phase Synthesis of Peptide C-Terminal Thioesters by Fmoc/t-Bu Chemistry
3. Fmoc-Based Synthesis of Peptide-αThioesters: Application to the Total Chemical Synthesis of a Glycoprotein by Native Chemical Ligation
4. Fmoc Solid-Phase Synthesis of Peptide Thioesters Using an Intramolecular N,S-Acyl Shift
5. Fmoc-Compatible Solid-Phase Peptide Synthesis of Long C-Terminal Peptide Thioesters
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1. Leveraging the Mukaiyama oxidation–reduction condensation reaction for on-resin aryl thio-esterification for bio-conjugation;Organic & Biomolecular Chemistry;2024
2. N-Sulfanylethylaminooxybutyramide (SEAoxy): A Crypto-Thioester Compatible with Fmoc Solid-Phase Peptide Synthesis;Organic Letters;2016-11-02
3. Protein Chemical Synthesis in Drug Discovery;Protein Ligation and Total Synthesis I;2014
4. An Fmoc Compatible, O to S Shift-Mediated Procedure for the Preparation of C-Terminal Thioester Peptides;The Journal of Organic Chemistry;2013-09-19
5. Preparation of Peptide Thioesters through Fmoc-Based Solid-Phase Peptide Synthesis by Using Amino Thioesters;European Journal of Organic Chemistry;2013-07-18
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