Iron-Catalyzed Stereoselective Nitrogen Atom Transfer for 1,2-cis-Selective Glycosylation

This account highlights an iron-catalyzed exclusively 1,2-<i>cis</i>-selective glycosylation method for aminoglycoside synthesis. This selective nitrogen atom transfer reaction is effective for a broad range of glycosyl donors and acceptors, and it can be operated in a reiterative fashion and scaled up to the multi-gram scale. Mechanistic studies revealed a unique yet generally applicable glycosylation mechanism in which the iron catalyst activates a glycosyl acceptor and an oxidant when it facilitates the cooperative atom transfer of both moieties to a glycosyl donor in an exclusively <i>cis</i>-selective manner.

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Publication Details

Journal
Synlett
Published
2025-07-14
DOI
https://doi.org/10.1055/a-2654-5609
Citations
4
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
Field-Weighted Citation Impact
3.74

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Iron-Catalyzed Stereoselective Nitrogen Atom Transfer for 1,2-cis-Selective Glycosylation

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article

Iron-Catalyzed Stereoselective Nitrogen Atom Transfer for 1,2-cis-Selective Glycosylation

Hao Xu, Le Yin, Pinzhi Wang, Zhonghao Jiang, Spencer A. Clark, Zhang Da-kang, Adam Cohen, Jordan D. Lamar
article en
4 citations

Abstract

This account highlights an iron-catalyzed exclusively 1,2-<i>cis</i>-selective glycosylation method for aminoglycoside synthesis. This selective nitrogen atom transfer reaction is effective for a broad range of glycosyl donors and acceptors, and it can be operated in a reiterative fashion and scaled up to the multi-gram scale. Mechanistic studies revealed a unique yet generally applicable glycosylation mechanism in which the iron catalyst activates a glycosyl acceptor and an oxidant when it facilitates the cooperative atom transfer of both moieties to a glycosyl donor in an exclusively <i>cis</i>-selective manner.

SynlettVol. 36(19)
Brandeis University (US)
National Institute of General Medical Sciences
Openalex Percentile: Top 7%
Carbohydrate Chemistry and Synthesis
3.74
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