One-step synthesis of β-C-glycolipid derivatives from unprotected sugars - Archive ouverte HAL
Article Dans Une Revue Carbohydrate Research Année : 2004

One-step synthesis of β-C-glycolipid derivatives from unprotected sugars

Résumé

Condensations of nonsymmetrical or symmetrical β-diketones and unprotected sugars in aq NaHCO3 soln were explored. C-glucosyl and C-maltosyl derivatives bearing lipophilic residue of 8 or 11 carbon atoms were prepared efficiently using this one-step procedure. The amphiphilic properties of these compounds were demonstrated by measuring their CMC.

Dates et versions

hal-03739740 , version 1 (28-07-2022)

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Yaël Hersant, Robert Abou-Jneid, Yves Canac, André Lubineau, Michel Philippe, et al.. One-step synthesis of β-C-glycolipid derivatives from unprotected sugars. Carbohydrate Research, 2004, 339 (3), pp.741-745. ⟨10.1016/j.carres.2003.11.007⟩. ⟨hal-03739740⟩
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