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.
Authors
- Eoghan M. McGarrigle (ORCID: https://orcid.org/0000-0001-8160-6431)
- Imlirenla Pongener (ORCID: https://orcid.org/0000-0002-1252-9396)
- Dionissia A. Pepe (ORCID: https://orcid.org/0000-0001-5401-8407)
- Chennaiah Ande
- Oana G. Popa
Institutions
- University College Dublin (IE)
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
- Field-Weighted Citation Impact
- 0.00