N-Arylation of Amino Acid Esters to Expand Side Chain Diversity in Ketoxime Peptide Ligations
Author:
Affiliation:
1. Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695-8204, United States
Funder
North Carolina State University
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02810
Reference48 articles.
1. Residue-Specific Peptide Modification: A Chemist’s Guide
2. Advances in Chemical Protein Modification
3. C–H Functionalization in the Synthesis of Amino Acids and Peptides
4. Modular Total Synthesis of Protein Kinase C Activator (−)-Indolactam V
5. Accelerating Effect Induced by the Structure of α-Amino Acid in the Copper-Catalyzed Coupling Reaction of Aryl Halides with α-Amino Acids. Synthesis of Benzolactam-V8
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