74629-63-3Relevant articles and documents
Glucosylation of 4′-hydroxychalcones using glucosyl donor
Ingle,Kharche,Upadhyay
, p. 801 - 805 (2007/10/03)
Condensation of α-acetobromoglucose with 4′- hydroxyarylmethyleneacetophenone derivatives (chalcones) in anhydrous acetone furnishes 2,3,4,6-tetra-O-acetyl-4′-O-β-D-glucopyranosyloxychalcones. Deblocking of the latter with CH3ONa in dry methanol affords 4′-O-β-D-glucopyranosyloxychalcones. The structure of these products have been assigned on the basis of their sophisticated instrumental analysis like IR, 1H NMR, 13C NMR, FAB-MS, specific rotation, elemental analysis and chemical properties.