Incorporation of Acid-Labile Masking Groups for the Traceless Synthesis of C-Terminal Peptide α-Ketoacids
Author:
Affiliation:
1. Laboratorium für Organische Chemie, Department of Chemistry and Applied Biosciences, ETH-Zürich, 8093 Zürich, Switzerland
2. Institute of Transformative bio-Molecules (WPI−ITbM), Nagoya University, Chikusa, Nagoya 464-8602, Japan
Funder
Ministry of Education, Culture, Sports, Science, and Technology
Swiss National Science Foundation
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b01692
Reference13 articles.
1. Chemical Protein Synthesis with the KAHA Ligation
2. Expanding the chemical toolbox for the synthesis of large and uniquely modified proteins
3. Synthesis of Proteins by Native Chemical Ligation
4. Chemical Synthesis of the 20 kDa Heme Protein Nitrophorin 4 by α‐Ketoacid‐Hydroxylamine (KAHA) Ligation
5. An oxazetidine amino acid for chemical protein synthesis by rapid, serine-forming ligations
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