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Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives Full article

Journal Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Output data Year: 2014, Volume: 24, Number: 6, Pages: 336-337 Pages count : 2 DOI: 10.1016/j.mencom.2014.11.006
Authors Krylov Vadim B. 1 , Argunov Dmitry A. 1 , Nifantiev Nikolay E. 1
Affiliations
1 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991,Moscow, Russian Federation

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.
Cite: Krylov V.B. , Argunov D.A. , Nifantiev N.E.
Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives
Mendeleev Communications. 2014. V.24. N6. P.336-337. DOI: 10.1016/j.mencom.2014.11.006 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000347139100006
≡ Scopus: 2-s2.0-84911935133
≡ OpenAlex: W1996452709
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