The Distal Effect of Electron-Withdrawing Groups and Hydrogen Bonding on the Stability of Peptide Enolates
Author:
Affiliation:
1. ARC Centre of Excellence for Free Radical Chemistry and Biotechnology, Research School of Chemistry, Australian National University, Canberra ACT 0200, Australia
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja100996z
Reference55 articles.
1. Structure and Reactivity of Lithium Enolates. From Pinacolone to SelectiveC-Alkylations of Peptides. Difficulties and Opportunities Afforded by Complex Structures
2. Posttranslational amino acid epimerization: enzyme-catalyzed isomerization of amino acid residues in peptide chains.
3. Biosynthesis of a D-amino acid in peptide linkage by an enzyme from frog skin secretions
4. Substrate Specificity of Platypus Venom L-to-D-Peptide Isomerase
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