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Microwave in glycosylation reaction: design, and synthesis of highly substituted nicotinonitrile nucleosides
Faculty
Science
Year:
2018
Type of Publication:
ZU Hosted
Pages:
10
Authors:
Ahmed Heussein Mostafa
Staff Zu Site
Abstract In Staff Site
Journal:
Computer Methods and Programs in Biomedicine ٍspringer
Volume:
153
Keywords :
Microwave , glycosylation reaction: design, , synthesis , highly substituted
Abstract:
An efficient and rapid regiospecific approach for the synthesis of cyclic and acyclic nucleosides of 2-oxonicotinonitriles was performed. Whereas, glycosylation of 2-oxonicotinonitriles 1a, b with peracetylated sugars (namely, peracetylate
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Department Related Publications
Mohamed Gamal Helmy Mohamed Abdelwahed, "Electronic Properties of Organic Complexes. 2. Reactive Azodyes", Spain, 1993
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Hamdy Aldedamony , "Studies on Portland Blast-Furnace Slag Cement with Limestone as a Retarder”", Indian J. Eng. & Sci, 1995
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Hamdy Aldedamony , "Resistivity of an Artificial Pozzolanic Cement to Chloride Solutions”", Silic. Ind.,, 1994
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Ragaa Sheikh Shuhaib, "Utility of Oxidation-Reduction Reaction for Determination of Gemifloxacin Mesylate and Moxifloxacin HCl in Pure Form and in Pharmaceutical Formulations using N-Bromosuccinimide", OMICS Publishing Group, 2013
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Ayman AboulFotouh Gouda Sallem, "Spectophotometricmethods for determination of cefdinir in pharmaceutical formulations via derivatization with 1,2-naphthoquinone-4-sulfonate and 4-chloro-7-nitrobenzo-2-oxa-1, 3-diazole", Wiley Online Library, 2011
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