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Synthesis of α-d-galactopyranosyl-linked oligosaccharides containing the α-Gal → β-Gal → GlcNAc sequence employing methyl-2,3,4,6-tetra-O-(4-methoxybenzyl)-1-thio- β-d-galactopyranoside as an efficient glycosyl donor

  • Roswell Park Cancer Institute

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

Synthesis of two trisaccharides and a tetrasaccharide, namely, α-Gal-(1 → 3)- β-Gal-(1 → 3)-GlcNAc-β-OBn (6), α-Gal-(1 → 3)-β-Gal-(1 → 4)-GlcNAc- β-OBn (9) and α-Gal-(1 → 3)-β-Gal-(1 → 4)-GlcNAc-β-(1 → 6)-GalNAc- α-OBn (19) was accomplished through development and utilization of a key α- galactosyl donor, methyl 2,3,4,6-tetra-O-(4-methoxybenzyl)-1-thio-β-d- galactopyranoside (1).

Original languageEnglish
Pages (from-to)67-77
Number of pages11
JournalCarbohydrate Research
Volume263
Issue number1
DOIs
StatePublished - Oct 3 1994

Keywords

  • Glycosyl donor
  • Synthesis of α-d-galactopyranosyl-linked oligosaccharides

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