Solid-phase synthesis of C-terminal peptide aldehydes from amino acetals anchored to a backbone amide linker (BAL) handle

Fanny Guillaumie, Joseph C. Kappel, Nicholas M. Kelly, George Barany, Knud J. Jensen

Research output: Contribution to journalArticlepeer-review

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Abstract

Peptide aldehydes were synthesized, starting from amino acetals, by a Solid-phase backbone amide linker (BAL) strategy.

Original languageEnglish (US)
Pages (from-to)6131-6135
Number of pages5
JournalTetrahedron Letters
Volume41
Issue number32
DOIs
StatePublished - Aug 5 2000

Bibliographical note

Funding Information:
We are grateful to Annette Nordestgaard from Phytera Symbion for LC/MS analyses, and Professor Fernando Albericio for valuable discussions. We thank the Leo Foundation (K.J.), the Lundbeck Foundation (K.J.), and the NIH (GM 42722 to GB) for financial support. J.K. was supported by an NIH Biotechnology Training Grant (GM 08347).

Keywords

  • Amino acetals
  • BAL
  • Peptide aldehydes
  • Solid-phase synthesis

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