The remarkable sensitivity to acid-catalyzed peptolysis of peptide chains (endopeptolysis) having a succession of three N-alkylated amino acid residues
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1988.tb00038.x/fullpdf
Reference19 articles.
1. Racemization during peptide coupling with N,N'-bis(2-oxo-3-oxazolidinyl) phosphinic chloride (BOP-Cl)
2. N,N'-bis(2-oxo-3-oxazolidinyl) phosphinic chloride (BOP-Cl); a superb reagent for coupling at and with iminoacid residues
3. Note on the Preparation of Very Active N,N-Bis (2-OXO-3-Oxazolidinyl)-Phosphorodiamidic Chloride (Bop-Cl), an extremely Effective Reagent for Peptide Formation
4. Preferential Release of Aspartic Acid During the Hydrolysis of Proteins
5. Easy cleavage of C′-terminal iminoacids from peptide acids through acidic hydrolysis
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