Conversion of serine and threonine residues into α-acyloxy-, a-alkylthio-, and α- halogenoglycine moieties: A new strategy for the modification of peptides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Selective modification of glycine residues in dipeptides
2. Selective reaction of glycine residues in hydrogen atom transfer from amino acid derivatives
3. Regioselective anodic oxidation of N ‐acyl, N ‐alkoxycarbonyl, and N ‐(2‐Nitrophenylsulfenyl) dipeptide esters
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