Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Fatma K. Abdel-Wadood"'
Autor:
Waleed Ahmed El-Said, Osama Nasr, Ahmed I. A. Soliman, Emad A. Elshehy, Ziya Ahmad Khan, Fatma K. Abdel-Wadood
Publikováno v:
Applied Surface Science Advances, Vol 4, Iss , Pp 100065- (2021)
Paracetamol (PC) is one of the most common non-steroidal anti-inflammatories, pain-killer, and antipyretic drugs. Thus, the development of a cheap, access, and accurate analytical technique is necessary for monitoring the purity of the PC in their ph
Externí odkaz:
https://doaj.org/article/541c35c6393442458d8b980bd88fbd58
Autor:
Shaaban K. Mohamed, El Hassane Anouar, Sajjad Ahmad, Mohamed S. Abbady, Fatma K. Abdel-Wadood, Maha Q. M. Qahtan, Joel T. Mague, Youness El Bakri
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f99794e9bc98ba15c302acd3bfafc181
https://doi.org/10.1080/07391102.2023.2180432
https://doi.org/10.1080/07391102.2023.2180432
Autor:
null Adel M. Kamal El-Dean, Ahmed A. Geies, Reda Hassanien, Fatma K. Abdel-Wadood, Eman E. Abd El-Naeem
Publikováno v:
Russian Journal of Bioorganic Chemistry. 48:821-834
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b2929725e7ce102ad39721db552e3f1
https://doi.org/10.1134/s1068162022040021
https://doi.org/10.1134/s1068162022040021
Autor:
Ahmed I. A. Soliman, Fatma K. Abdel-Wadood, Osama Nasr, Ziya Ahmad Khan, Emad A. Elshehy, Waleed A. El-Said
Publikováno v:
Applied Surface Science Advances, Vol 4, Iss, Pp 100065-(2021)
Paracetamol (PC) is one of the most common non-steroidal anti-inflammatories, pain-killer, and antipyretic drugs. Thus, the development of a cheap, access, and accurate analytical technique is necessary for monitoring the purity of the PC in their ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f48fce408a14bd9ea381340be9a19cec
http://www.sciencedirect.com/science/article/pii/S2666523921000118
http://www.sciencedirect.com/science/article/pii/S2666523921000118
Publikováno v:
Archiv der Pharmazie. 347:142-152
2-Bromo-4-fluoroaniline (1) was condensed with ethyl 2-cyano-3-ethoxyacrylate (2) in ethanol to afford 3, which upon refluxing in paraffin oil at 250°C gave 8-bromo-3-cyano-6-fluoroquinoline-4(1H)-one (4). Then, compound 4 was taken as a versatile b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::756b6fdd7965cf863b082698475714f1
https://doi.org/10.1002/ardp.201300167
https://doi.org/10.1002/ardp.201300167
Publikováno v:
Journal of Chemical Research. 2008:89-94
3-Cyano-6-methyl-5,6,7,8-tetrahydro[1,6]naphthyridine-2(1H)-thione (3a) and 3-cyano-6-methyl-4-(2′-thienyl)-5,6,7,8-tetrahydro[1,6]naphthyridine-2(1H)-thione (3b) were reacted with α-halo compounds to give the intermediates 4a–j which upon reflu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ff1690f7b280c92d0750d431362f6b7
https://doi.org/10.3184/030823408784365306
https://doi.org/10.3184/030823408784365306
Publikováno v:
ChemInform. 39
Fatma K. Abdel-Wadood, Maisa I. Abdel-Monem, Atiat M. Fahmy, and Ahmed A. Geies Chemistry Department, Faculty of Science, Assiut University, Assiut 71516, Egypt Reprint requests to Prof. Dr. Ahmed Geies. Fax: 0020882342708. E-mail: geies@aun.edu.eg Z
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::004cc76ffaf986c6aff9e487a83beb91
https://doi.org/10.1002/chin.200827035
https://doi.org/10.1002/chin.200827035
Publikováno v:
Archiv der Pharmazie. 347(2)
2-Bromo-4-fluoroaniline (1) was condensed with ethyl 2-cyano-3-ethoxyacrylate (2) in ethanol to afford 3, which upon refluxing in paraffin oil at 250°C gave 8-bromo-3-cyano-6-fluoroquinoline-4(1H)-one (4). Then, compound 4 was taken as a versatile b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5c7cecc7646967d45ed2c0f42133347c
https://pubmed.ncbi.nlm.nih.gov/24375769
https://pubmed.ncbi.nlm.nih.gov/24375769
Publikováno v:
ChemInform. 39
3-Cyano-6-methyl-5,6,7,8-tetrahydro[1,6]naphthyridine-2(1H)-thione (3a) and 3-cyano-6-methyl-4-(2'-thienyl)-5,6,7,8- tetrahydro[1,6]naphthyridine-2(1H)-thione (3b) were reacted with α-halo compounds to give the intermediates 4a-j which upon refluxin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfb384a62291deb76ed56ba806548a2f
https://doi.org/10.1002/chin.200838148
https://doi.org/10.1002/chin.200838148
Publikováno v:
Archiv der Pharmazie; Feb2014, Vol. 347 Issue 2, p142-152, 11p