A convenient procedure for the preparation of fully-protected C-terminal glycopeptides

Amy C. Bauman*, J. Scott Broderick, Robert M. Dacus IV, Danny A. Grover, Larry S. Trzupek

*Corresponding author for this work

Research output: Contribution to journalArticle

6 Scopus citations

Abstract

The acetic acid catalyed reaction of the free amine form of a glycosylated serine ester with amino acids or peptides built-up on a Kaiser-DeGrado polystyrene benzophenone oxime resin affords C-terminal glycopeptides in a fully-protected form suitable for further chemical manipulation.

Original languageEnglish (US)
Pages (from-to)7019-7022
Number of pages4
JournalTetrahedron Letters
Volume34
Issue number44
DOIs
StatePublished - Oct 29 1993

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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