Automated Synthesis of C1-Functionalized Oligosaccharides

Automated glycan assembly (AGA) streamlines the synthesis of complex oligosaccharides. The reducing end of the oligosaccharide serves as an attachment site to the polymer support to liberate a free reducing end or an aminopentanol for ready conjugation to carrier proteins or surfaces. The facile installation of different aglycons on oligosaccharides has not been possible via AGA until now. Here, we describe a latent-active approach enabled by a traceless photolabile linker that allows for bidirectional AGA and ready introduction of various aglycons. Oligosaccharide thioglycosides, peptidoglycans, prototypical saponins, and click-chemistry-based conjugates are synthesized to illustrate the versatility of the method.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-12-31
DOI
https://doi.org/10.1021/jacs.4c11798
Citations
5
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
Field-Weighted Citation Impact
1.25

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article

Automated Synthesis of C1-Functionalized Oligosaccharides

Georg Niggemeyer, Peter H. Seeberger, José Danglad‐Flores
5 citations
Journal of the American Chemical Society
Carbohydrate Chemistry and Synthesis
1.25
article

Automated Synthesis of C1-Functionalized Oligosaccharides

Georg Niggemeyer, Peter H. Seeberger, José Danglad‐Flores
article en
5 citations

Abstract

Automated glycan assembly (AGA) streamlines the synthesis of complex oligosaccharides. The reducing end of the oligosaccharide serves as an attachment site to the polymer support to liberate a free reducing end or an aminopentanol for ready conjugation to carrier proteins or surfaces. The facile installation of different aglycons on oligosaccharides has not been possible via AGA until now. Here, we describe a latent-active approach enabled by a traceless photolabile linker that allows for bidirectional AGA and ready introduction of various aglycons. Oligosaccharide thioglycosides, peptidoglycans, prototypical saponins, and click-chemistry-based conjugates are synthesized to illustrate the versatility of the method.

Journal of the American Chemical SocietyVol. 147(2)
Max Planck Institute of Colloids and Interfaces (DE), Freie Universität Berlin (DE)
Max-Planck-Gesellschaft
Openalex Percentile: Top 21%
Carbohydrate Chemistry and Synthesis
1.25
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Automated Synthesis of C1-Functionalized Oligosaccharides — Georg Niggemeyer, Peter H. Seeberger, et al. · Journal of the American Chemical Society (2024) | TGRS Research Map | TGRS