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Mendeleev Communications, 2014, Volume 24, Issue 6, Pages 336–337
DOI: https://doi.org/10.1016/j.mencom.2014.11.006
(Mi mendc2571)
 

This article is cited in 7 scientific papers (total in 7 papers)

Communications

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

V. B. Krylov, D. A. Argunov, N. E. Nifantiev

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (314 kB) Citations (7)
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.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.1 Mb)


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/mendc/v24/i6/p336
  • This publication is cited in the following 7 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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