Synthesis of carbon-linked glycopeptides as stable glycopeptide models

Carolyn R. Bertozzi, Paul D. Hoeprich, Mark D. Bednarski

Research output: Contribution to journalArticle

83 Citations (Scopus)

Abstract

A C-glycosyl analog of β-Gal-O-Ser has been synthesized and incorporated by automated solid-phase peptide synthesis into a hydrolytically stable, α-helical C-glycopeptide.

Original languageEnglish (US)
Pages (from-to)6092-6094
Number of pages3
JournalJournal of Organic Chemistry
Volume57
Issue number23
StatePublished - 1992
Externally publishedYes

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Glycopeptides
Carbon
Peptides

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Bertozzi, C. R., Hoeprich, P. D., & Bednarski, M. D. (1992). Synthesis of carbon-linked glycopeptides as stable glycopeptide models. Journal of Organic Chemistry, 57(23), 6092-6094.

Synthesis of carbon-linked glycopeptides as stable glycopeptide models. / Bertozzi, Carolyn R.; Hoeprich, Paul D.; Bednarski, Mark D.

In: Journal of Organic Chemistry, Vol. 57, No. 23, 1992, p. 6092-6094.

Research output: Contribution to journalArticle

Bertozzi, CR, Hoeprich, PD & Bednarski, MD 1992, 'Synthesis of carbon-linked glycopeptides as stable glycopeptide models', Journal of Organic Chemistry, vol. 57, no. 23, pp. 6092-6094.
Bertozzi CR, Hoeprich PD, Bednarski MD. Synthesis of carbon-linked glycopeptides as stable glycopeptide models. Journal of Organic Chemistry. 1992;57(23):6092-6094.
Bertozzi, Carolyn R. ; Hoeprich, Paul D. ; Bednarski, Mark D. / Synthesis of carbon-linked glycopeptides as stable glycopeptide models. In: Journal of Organic Chemistry. 1992 ; Vol. 57, No. 23. pp. 6092-6094.
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