ISSN print edition: 0366-6352
ISSN electronic edition: 1336-9075
Registr. No.: MK SR 9/7

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Synthesis of the Inhibitors of Glycanases

T. Stach, M. Matulová, V. Farkaš, Z. Sulová, V. Pätoprstý, and K. Linek

Institute of Chemistry, Slovak Academy of Sciences, SK-842 38 Bratislava

 

Abstract: 2,3-Epoxypropyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside was obtained by oxidation of allyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside; deacetylation of the former compound afforded 2,3-epoxypropylacetyl-β-D-glucopyranoside, Analogous oxidation and deacetylation of allyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→4)-2,3,6-tri-O-acetyl-β-D-glucopyranoside produced 2,3-epoxypropyl 2,3,4,6-tetra- O-acetyl-β-D-glucopyranosyl-(1→4)-2,3,6-O-acetyl-β-D-glucopyranoside and 2,3-epoxypropyl β-D-glucopyranosyl-(1→4)-β-D-glucopyranoside respectively. Structure, anomeric and absolute configuration of these substances were determined by 1H and 13C NMR spectroscopic methods, and mass spectrometric methods. The deacetylated epoxyalkyl β-D-glycosides were effective as irreversible active-site directed inhibitors of β-glycosidase from sweet almonds.

Full paper in Portable Document Format: 533a218.pdf

 

Chemical Papers 53 (3) 218–223 (1999)

Wednesday, November 13, 2019

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