الفهرس 
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Abstract
Abstract4,6-Diaryl-1-(2′,3′,4′,6′-tetra-O-acetyl-β-D-gluco/galactopyranosyloxy)pyridin-2-one-3-carbonitrile 3a-c, riboside 6a-c, and lactoside 9a-c were obtained by the reaction of 1a-c with glucosyl / galactosyl / actosyl bromide and peracetylated ribose under the conventional and microwave methods. Deprotection of 3a-c, 6a-c, and 9a-c in the presence of Et3N / MeOH and few drops of water afforded 4a-c, 7a-c and 10a-c. The structure of the new synthesized compounds was assigned by spectral and microanalysis data. Selected members of these compounds were screened for antiviral, antimicrobial activity NH O CN Ar’ Ar 1 a-c 2,5,8 / K2CO3 / DMF N O CN Ar’ Ar H2O N O CN Ar Ar’ Et3N / Methanol G G’ HMDS / SnCl4 3a-c 6a-c 9a-c 4a-c 7a-c 10a-c 2 = glucosyl / galactosyl bromide 5 = peracetylated ribose 8 = lactosyl bromide Where, G and G’ are: gluco, galacto, ribo, and Lacto moiety a-c, are a dif frent Ar and Ar’ substituents References 1- H. A. El-Sayed, A. H. Moustafa, A. Z. Haikal, R. A. El-Halaw, E. S. H. El Ashry, Eur. .J Med. Chem., 46 (2011), 2948-2954 2- A. H. Moustafa, H. A. Morsy, M. G. Assy, A. Z. Haikal, Nucleosides, Nucleotides & Nucleic Acids, 28