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- W2149679619 abstract "Decarboxylative allylation of glycals: A β-type glycosidic bond has been constructed in high regio- and stereoselectivity by means of a palladium-catalyzed decarboxylative O-glycosylation. Various kinds of glycals with different protecting groups have been examined for this reaction to afford a diverse set of glycosylated products, including phenolic O-glycosides, thiophenolic S-glycoside, aliphatic O-glycosides, and disaccharides with excellent β-selectivity and reasonable to excellent yields (see scheme). As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
- W2149679619 created "2016-06-24" @default.
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- W2149679619 date "2013-09-17" @default.
- W2149679619 modified "2023-10-12" @default.
- W2149679619 title "β-Type Glycosidic Bond Formation by Palladium-Catalyzed Decarboxylative Allylation" @default.
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- W2149679619 doi "https://doi.org/10.1002/chem.201303241" @default.
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