Abstract:
Heating of trisodium salt of allyl 3-O-benzyl-2,5,6-tri-O-sulfonato-β-D-galactofuranoside with pyridinium chloride in dioxane affords 1,6-anhydro-3-O-benzyl-α-D-galactofuranose which was regioselectively acylated to give useful precursors for oligosaccharide synthesis.
Citation:
V. B. Krylov, D. A. Argunov, N. E. Nifantiev, “Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives”, Mendeleev Commun., 24:6 (2014), 336–337
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https://www.mathnet.ru/eng/mendc2571
https://www.mathnet.ru/eng/mendc/v24/i6/p336
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