Chemoselective Amide Formation Using O-(4-Nitrophenyl)hydroxylamines and Pyruvic Acid Derivatives
Author:
Affiliation:
1. Department of Medical Education, College of Medicine, University of Central Florida, 6850 Lake Nona Boulevard, Orlando, Florida 32827, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo302175g
Reference46 articles.
1. Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of Functionality
2. Chemoselective Amide Ligations by Decarboxylative Condensations ofN-Alkylhydroxylamines and α-Ketoacids
3. Iterative, Aqueous Synthesis of β3-Oligopeptides without Coupling Reagents
4. Stereoretentive Synthesis and Chemoselective Amide-Forming Ligations of C-Terminal Peptide α-Ketoacids
5. The Mechanism of the α-Ketoacid-Hydroxylamine Amide-Forming Ligation
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