Publication | Closed Access
Chiral Isocyanoazides: Efficient Bifunctional Reagents for Bioconjugation
65
Citations
29
References
2010
Year
EngineeringBiochemistryPeptide EngineeringHybrid Peptide MoleculesTriazole DerivativesAzide GroupsOrganic ChemistryPeptide SciencePeptide SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringChiral Isocyanoazides
Abstract Chiral scaffolds combining isocyanide and azide groups can be effectively synthesized to permit the efficient construction of both amino (hydroxy) acids and triazole derivatives, which enables the preparation of hybrid peptide molecules by Ugi/click or click/Ugi strategies.
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