Peptide Bond Formation of Amino Acids by Transient Masking with Silylating Reagents
Wataru Muramatsu, Hisashi Yamamoto
Abstract
A one-pot peptide bond-forming reaction has been developed using unprotected amino acids and peptides. Two different silylating reagents, HSi[OCH(CF3)2]3 and MTBSTFA, are instrumental for the successful implementation of this approach, being used for the activation and transient masking of unprotected amino acids and peptides at C-termini and N-termini, respectively. Furthermore, CsF and imidazole are used as catalysts, activating HSi[OCH(CF3)2]3 and also accelerating chemoselective silylation. This method is versatile as it tolerates side chains that bear a range of functional groups, while providing up to >99% yields of corresponding peptides without any racemization or polymerization.
Topics & Concepts
ChemistryReagentRacemizationAmino acidSilylationPeptideCombinatorial chemistryMasking (illustration)PolymerizationPeptide bondImidazolePeptide synthesisCatalysisOrganic chemistryPolymerBiochemistryArtVisual artsChemical Synthesis and AnalysisFluorine in Organic ChemistryAsymmetric Synthesis and Catalysis