Journal
CHEMICAL COMMUNICATIONS
Volume 54, Issue 34, Pages 4337-4340Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cc01965g
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Funding
- Japan Society for the Promotion of Science (JSPS) [15H02190]
- Grants-in-Aid for Scientific Research [15H02190] Funding Source: KAKEN
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An efficient method for peptide ligation between C-terminal Asp(OAllyl) and N-terminal Cys has been developed. Peptide ligation and removal of the allyl group at the Asp carboxylate side chain proceeded in one pot by adding a small amount of Pd/TPPTS complex. Based on this efficient synthetic method, PEP-19 (61 amino acids), which is highly expressed in Purkinje cells, was synthesized.
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