Stereoselective α-Glucosylations from Glycosyl Hemiacetals Mediated by Lithium Iodide and Synthesis of the Pentasaccharide Repeating Unit of FPS-1

A stereoselective synthesis of 1,2-<i>cis-</i>glucosides from glucosyl hemiacetals is reported herein. It proceeds through a one-pot chlorination (under Appel conditions), halide metathesis to iodide (with LiI), and glycosylation sequence. A range of glycosyl acceptors and donors is shown to be suitable under the reaction conditions. To demonstrate the utility of this method, a target pentasaccharide containing 4 α-glucosyl linkages was synthesized.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-02-06
DOI
https://doi.org/10.1021/acs.joc.5c02828
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
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article

Stereoselective α-Glucosylations from Glycosyl Hemiacetals Mediated by Lithium Iodide and Synthesis of the Pentasaccharide Repeating Unit of FPS-1

Eoghan M. McGarrigle, Imlirenla Pongener, Dionissia A. Pepe, Chennaiah Ande et al.
The Journal of Organic Chemistry
Carbohydrate Chemistry and Synthesis
article

Stereoselective α-Glucosylations from Glycosyl Hemiacetals Mediated by Lithium Iodide and Synthesis of the Pentasaccharide Repeating Unit of FPS-1

Eoghan M. McGarrigle, Imlirenla Pongener, Dionissia A. Pepe, Chennaiah Ande, Oana G. Popa
article en

Abstract

A stereoselective synthesis of 1,2-<i>cis-</i>glucosides from glucosyl hemiacetals is reported herein. It proceeds through a one-pot chlorination (under Appel conditions), halide metathesis to iodide (with LiI), and glycosylation sequence. A range of glycosyl acceptors and donors is shown to be suitable under the reaction conditions. To demonstrate the utility of this method, a target pentasaccharide containing 4 α-glucosyl linkages was synthesized.

The Journal of Organic ChemistryVol. 91(7)
University College Dublin (IE)
Clean water and sanitation
Openalex Percentile: Top 64%
Carbohydrate Chemistry and Synthesis
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