Visible‐Light Mediated Tryptophan Modification in Oligopeptides Employing Acylsilanes
Jannik Reimler, Armido Studer
Abstract
A method for the selective tryptophan modification and labelling of tryptophan-containing peptides is described. Photoirradiation of acylsilanes generates reactive siloxycarbenes which undergo H-N-insertion into the indole moiety of tryptophan to give stable silyl protected hemiaminals. This method is successfully applied to chemically modify various tryptophan containing oligopeptides. The method enables the selective introduction of alkynes to peptides that are eligible for further alkyne-azide click chemistry. In addition, the dansyl fluorophore can be conjugated to a peptide using this approach.
Topics & Concepts
TryptophanMoietyIndole testFluorophoreChemistryConjugated systemOligopeptideCombinatorial chemistryAlkyneAzideClick chemistryPeptideFluorescenceStereochemistryOrganic chemistryBiochemistryAmino acidCatalysisPhysicsPolymerQuantum mechanicsClick Chemistry and ApplicationsChemical Synthesis and AnalysisFluorine in Organic Chemistry