Recent carbohydrate-based chemoselective ligation applications

Joseph M. Langenhan, Jon S. Thorson

Research output: Contribution to journalReview articlepeer-review

76 Scopus citations

Abstract

Chemoselective ligation reactions are highly efficient and specific covalent bond forming reactions capable of proceeding within a physiological environment. Chemoselective ligations offer exquisite specificity, similar to enzymatic reactions, but with the significant advantage of accessing a much broader range of coupling partners. Thus, even among a multitude of reactive functional groups, two ligation partners exclusively react with one another. While chemoselective ligation has been used in many applications, the focus of this review is the application of chemoselective ligation reactions toward carbohydrate-based structures. More specifically, recent applications are presented in areas such as immobilized carbohydrate arrays, cell-surface engineering, glycoproteins/peptides, and glycosylated natural products.

Original languageEnglish
Pages (from-to)59-81
Number of pages23
JournalCurrent Organic Synthesis
Volume2
Issue number1
DOIs
StatePublished - Jan 2005

Keywords

  • Chemoselective ligation
  • Cycloadditions
  • Diels-alder reactions
  • Oligosaccharides

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry

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