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Article dans une revue

Solvent- and catalyst-free transamidations of unprotected glycosyl carboxamides

Abstract : The transamidation reactions of unprotected mono- and disaccharidic carboxamides with various primary and secondary arylic, heterocyclic or aliphatic amines are described. This new method is green and atom efficient and gives good to high yields. Notably, the conditions do not require either a solvent or a catalyst and give ammonia as a single by-product. The described coupling reaction is compatible with a variety of functional groups and was used in the synthesis of various glycosidic derivatives and biologically relevant glycolipids. A plausible reaction mechanism involving an intermolecular H-bond activation of the starting carboxamides is proposed.
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https://hal-u-picardie.archives-ouvertes.fr/hal-03613738
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Soumis le : vendredi 18 mars 2022 - 16:48:22
Dernière modification le : mardi 27 septembre 2022 - 04:32:43

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Fouzia Ouadah Bensalah, Abed Bil, Karlo Wittine, Salima Bellahouel, David Lesur, et al.. Solvent- and catalyst-free transamidations of unprotected glycosyl carboxamides. Organic & Biomolecular Chemistry, Royal Society of Chemistry, 2019, 17 (43), pp.9425-9429. ⟨10.1039/c9ob02096a⟩. ⟨hal-03613738⟩

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