Peptide Ligation via the Suzuki-Miyaura Cross-Coupling Reaction

Tae Kyung Lee, Bikash Manandhar, Kara J. Kassees, Jung Mo Ahn

Research output: Contribution to journalArticlepeer-review

4 Scopus citations


Chemoselective ligation of two 28-mer peptides has been accomplished using the Suzuki-Miyaura cross-coupling reaction at or near physiological temperature in an aqueous solution containing sodium dodecyl sulfate in 83% yield. The effects of Pd source, solvent, base, and temperature were investigated, and the optimized reaction conditions were studied for compatibility with naturally present and artificially introduced functional groups in peptides including S-protected thiol and azide. The peptide conjugations were carried out in high yield (90%) with their functional groups intact. This method also allowed for facile introduction of an affinity tag or fluorescent probe into 20-mer peptides in >80% yield. These results suggest that the Suzuki-Miyaura cross-coupling is useful for multiple conjugations of peptides in conjunction with conventional conjugation reactions performed in sequence.

Original languageEnglish (US)
Pages (from-to)1376-1384
Number of pages9
JournalJournal of Organic Chemistry
Issue number3
StatePublished - Feb 7 2020
Externally publishedYes

ASJC Scopus subject areas

  • Organic Chemistry


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