O- and N-acylureas in peptide synthesis by DCC method. New observations
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. A New Method of Forming Peptide Bonds
2. Isolation and reactivity of a model for the carbodiimide-carboxylic acid adduct. O-Benzoyl-N,N-dimethyl-N'-(N-methyl-2,4-dinitroanilino)isourea
3. A simplified method for the determination of racemization and by-product formation in peptide synthesis
4. A. Kołodziejczyk, A. Arendt, Pol. J. Ghem., in press.
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1. Peptide-Coupling Reagents;Amino Acids, Peptides and Proteins in Organic Chemistry;2011-01-31
2. Formation of N-(1-ferrocenoylpyrrolidine-2-carbonyl)-N,N′-dicyclohexylurea: Dead-end in the preparation of ferrocene-modified peptides;Inorganica Chimica Acta;2009-08
3. Reaction of an introverted carboxylic acid with carbodiimide;Tetrahedron;2007-07
4. NEW TRENDS IN PEPTIDE COUPLING REAGENTS;Organic Preparations and Procedures International;2001-06
5. Synthesis of coumarin-3-O-acylisoureas by dicyclohexylcarbodiimide;Journal of Heterocyclic Chemistry;1995-03
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