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Expansion of Phosphane Treasure Box for Staudinger Peptide Ligation

Kiran Bajaj, Girinath G. Pillai, Rajeev Sakhuja, Dalip Kumar

2020The Journal of Organic Chemistry11 citationsDOI

Abstract

A smooth traceless ligation strategy using an air-stable phosphane probe (2-(diphenylphosphanyl)phenyl)methanol as a C-terminus activator has been demonstrated at simple and sterically hindered amino acid junctions (Gly, Ala, Trp, Glu). This Staudinger peptide ligation proceeds via formation of a seven-membered transition state to afford di-, tetra-, and pentapeptides in 78-95% yields. The experimental results of ligation at Gly junction and regioselective ligation at Glu junction were theoretically studied by computational calculations. These findings established the versatile behavior of our synthesized phosphane probe for Staudinger peptide ligation toward synthesizing peptides and proteins of choice.

Topics & Concepts

ChemistryChemical ligationLigationPeptideStaudinger reactionCombinatorial chemistrySteric effectsStereochemistryBiochemistryMolecular biologyBiologyChemical Synthesis and AnalysisClick Chemistry and ApplicationsCarbohydrate Chemistry and Synthesis
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