Fawzy A. Attaby

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6-Aryl-5-cyano-4-pyrimidinon-2-thione derivatives1a-c reacted with ethyl iodide to give the corresponded 2-S-ethylpyrimidin-4-one derivatives2a-c. Compounds2a-c was, in turn, reacted with hydrazine hydrate to give the sulfur free reaction products,3a-c. These reaction products were taken as the starting materials for the synthesis of several newly(More)
The reaction of thiocyanoacetamide (1) with alpha,beta-unsaturated ketones 2a,b resulted in the formation of the corresponding newly synthesized 1(H)-pyridinethione derivatives 3a,b. Compounds 3a,b were used as synthons for the preparation of 2-S-alkyl-, 2-S-aryl-, 2-S-acetamidopyridine, thieno[2,3-b]pyridine and pyrazolo[3,4-b]pyridine derivatives via a(More)
This study aimed for the synthesis of new heterocyclic compounds incorporating sulfamoyl moiety suitable for use as antimicrobial agents via a versatile, readily accessible N-[4-(aminosulfonyl)phenyl]-2-cyanoacetamide (3). The 2-pyridone derivatives were obtained via reaction of cyanoacetamide with acetylacetone or arylidenes malononitrile. Cycloaddition(More)
Thiocarboxamidocinnamonitrile derivatives2 a-f reacted with 3-aminopyrazole derivatives3 a-c to give the pyrazole[3,2-b]pyrimidine derivatives6 a-p. Compounds6 a-p were used as starting material for syntheses of several heterocylic coompounds. Dehydrogenation of6 gave pyrazole[3,2-b]pyrimidines10 a-d while its reaction with diethyl oxalate gave11. Reactions(More)
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