Development, Scope, and Catalyst Selection in Boron-Catalyzed Iterative Glycosylation

Boron-catalyzed glycosylations provide an effective strategy for the rapid and simple preparation of glycosidic bonds by using glycosyl fluoride donors and silyl ether acceptors. This study examines the utility of this reaction type in iterative glycosylations, where the sequence of formation of glycosidic bonds with silyl ether acceptors is governed by a trialkyl silane structure rather than the inherent reactivity of the hydroxyl precursors. Relative rates and selectivities of glycosylations were studied by <sup>19</sup>F NMR, identifying BF<sub>3</sub>·OEt<sub>2</sub> as an excellent catalyst choice for iterative processes. Using this protocol, a number of site-selective and stereoselective iterative glycosylations were demonstrated to produce tri- and tetrasaccharides from monosaccharide precursors, and more complex examples were prepared by related stepwise approaches.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-12-08
DOI
https://doi.org/10.1021/jacs.5c14412
Citations
1
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
Field-Weighted Citation Impact
0.94
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article

Development, Scope, and Catalyst Selection in Boron-Catalyzed Iterative Glycosylation

Girish C. Sati, Kishor R. Harale, Taylor E. Spiller, Annabel Q. Ansel et al.
1 citations
Journal of the American Chemical Society
Carbohydrate Chemistry and Synthesis
0.94
article

Development, Scope, and Catalyst Selection in Boron-Catalyzed Iterative Glycosylation

Girish C. Sati, Kishor R. Harale, Taylor E. Spiller, Annabel Q. Ansel, John Montgomery, Chandana Sunil, Joshua L. Martin, Timothy Emmel
article en
1 citations

Abstract

Boron-catalyzed glycosylations provide an effective strategy for the rapid and simple preparation of glycosidic bonds by using glycosyl fluoride donors and silyl ether acceptors. This study examines the utility of this reaction type in iterative glycosylations, where the sequence of formation of glycosidic bonds with silyl ether acceptors is governed by a trialkyl silane structure rather than the inherent reactivity of the hydroxyl precursors. Relative rates and selectivities of glycosylations were studied by <sup>19</sup>F NMR, identifying BF<sub>3</sub>·OEt<sub>2</sub> as an excellent catalyst choice for iterative processes. Using this protocol, a number of site-selective and stereoselective iterative glycosylations were demonstrated to produce tri- and tetrasaccharides from monosaccharide precursors, and more complex examples were prepared by related stepwise approaches.

Journal of the American Chemical SocietyVol. 147(50)
University of Michigan (US)
Openalex Percentile: Top 19%
Carbohydrate Chemistry and Synthesis
0.94
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