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Influence of Remote Picolinyl and Picoloyl Stereodirecting Groups for the Stereoselective Glycosylation

https://doi.org/10.1002/ajoc.202000558

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What this work says

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Straightforward sequential and one-pot synthesis of a pentasaccharide repeating unit corresponding to the cell wall O-antigen of Shigella boydii type 18

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Picolinyl group as an efficient alcohol protecting group: cleavage with Zn(OAc)2·2H2O under a neutral condition

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The Organic Chemistry of Sugars

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/chem.202401908openalex-snapshot

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inferred← citeshttps://doi.org/10.1002/ejoc.202300146openalex-snapshot

Kdo Glycosylations and Their Application in Oligosaccharide Synthesis**

inferred← citeshttps://doi.org/10.1002/ejoc.202301063openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/bs.accb.2022.10.003openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.carres.2026.109962openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.gresc.2024.03.004openalex-snapshot

Unraveling chemical glycosylation: DFT insights into factors imparting stereoselectivity

inferred← citeshttps://doi.org/10.1016/s1875-5364(23)60408-xopenalex-snapshot

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