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Rapid and Highly Productive Assembly of a Disulfide Bond in Solid-Phase Peptide Macrocyclization.

Arnab ChowdhuryVinod GourBasab Kanti DasSaurav ChatterjeeAnupam Bandyopadhyay
Published in: Organic letters (2023)
Here we report a highly efficient disulfide-driven peptide macrocyclization in 15 min on a solid support using persulfate as a crucial additive in iodine-mediated oxidative cyclization. The method eliminates the side products of classical iodine-mediated peptide cyclization. It is operationally simple and convenient for cyclizing small to lengthier peptides embodying popular cysteine building blocks in a single step.
Keyphrases
  • highly efficient
  • dual energy
  • magnetic resonance imaging
  • magnetic resonance
  • fluorescent probe
  • loop mediated isothermal amplification