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Synthesis of L-Hexopyranosyl Fluorides Enabled by Radical Decarboxylative Fluorination: Assembly of a Pentasaccharide Repeating Unit Corresponding to Extracellular Polysaccharide S-88
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  • Zhi Qiao,
  • Dongwei Li,
  • Jingru Gao,
  • Zijiao Hou,
  • Ningjie Yan,
  • Ni Song,
  • Peng Wang,
  • Ming Li
Zhi Qiao
Ocean University of China
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Dongwei Li
Ocean University of China
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Jingru Gao
Ocean University of China
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Zijiao Hou
Ocean University of China
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Ningjie Yan
Ocean University of China
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Ni Song
Ocean University of China
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Peng Wang
Ocean University of China
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Ming Li
Ocean University of China

Corresponding Author:[email protected]

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Abstract

L-Hexoses are key components of many biologically relevant natural products and pharmaceuticals. As rare sugars, L-hexoses are not readily obtained from natural sources. Access to L-hexose building blocks from commercially available and inexpensive D-sugars is highly desirable from the viewpoints of organic synthesis and drug discovery. As demonstrated by the convenient preparation of L-glucosyl, L-galactosyl, and L-mannosyl fluorides from readily available β-D-C-glucosyl, β-D-C-mannosyl, and β-D-C-galactosyl derivatives, we describe a novel and efficient approach to the demanding L-glycosyl fluorides. The transformation features the installation of anomeric hydroxymethyl group under mild conditions and head-to-tail inversion of sugar rings through radical decarboxylative fluorination of uronic acids. The power of this protocol is highlighted by the first assembly of a pentasaccharide repeating unit of Pseudomonas ATCC 31554 extracellular polysaccharide (S-88). This synthesis relies on the efficient extension of sugar chain at the sterically hindered hydroxy group and the facile introduction of L-mannosyl unit using L-mannosyl fluoride as glycosylating agent. The methods developed in this work would provide new tools to the arsenal of synthesis of L-sugar building blocks and of assembly of glycans containing L-sugar moieties.
27 Jul 20231st Revision Received
28 Jul 2023Submission Checks Completed
28 Jul 2023Assigned to Editor
28 Jul 2023Review(s) Completed, Editorial Evaluation Pending
28 Jul 2023Reviewer(s) Assigned
01 Aug 2023Editorial Decision: Accept
22 Aug 2023Published in Chinese Journal of Chemistry. 10.1002/cjoc.202300392