OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Synthesis, antibacterial activity and in silico study of new bis(1,3,4-oxadiazoles)
Ahmed Abdelfattah, Ahmed E. M. Mekky, Sherif M. H. Sanad
Synthetic Communications (2022) Vol. 52, Iss. 11-12, pp. 1421-1440
Closed Access | Times Cited: 13
Ahmed Abdelfattah, Ahmed E. M. Mekky, Sherif M. H. Sanad
Synthetic Communications (2022) Vol. 52, Iss. 11-12, pp. 1421-1440
Closed Access | Times Cited: 13
Showing 13 citing articles:
Synthesis of New Pyrazolo[1,5‐a]pyrimidines as Potential Antibacterial Agents: In Vitro and In Silico Study
Ahmed E. M. Mekky, Sherif M. H. Sanad
ChemistrySelect (2023) Vol. 8, Iss. 17
Closed Access | Times Cited: 10
Ahmed E. M. Mekky, Sherif M. H. Sanad
ChemistrySelect (2023) Vol. 8, Iss. 17
Closed Access | Times Cited: 10
New thiazole-based bis(Schiff bases) linked to arene units as potential MRSA inhibitors
Ahmed E. M. Mekky, Sherif M. H. Sanad
Synthetic Communications (2022) Vol. 52, Iss. 23, pp. 2205-2218
Closed Access | Times Cited: 9
Ahmed E. M. Mekky, Sherif M. H. Sanad
Synthetic Communications (2022) Vol. 52, Iss. 23, pp. 2205-2218
Closed Access | Times Cited: 9
An In‐Depth Review on Recent Progress in Synthetic Approaches and Biological Activities of Thiazol‐2(3H)‐Imine Derivatives
Arslan Saleem, Ghulam Shabir, Hummera Rafique, et al.
ChemistrySelect (2024) Vol. 9, Iss. 32
Open Access | Times Cited: 1
Arslan Saleem, Ghulam Shabir, Hummera Rafique, et al.
ChemistrySelect (2024) Vol. 9, Iss. 32
Open Access | Times Cited: 1
[3 + 2] Cycloaddition synthesis of new (nicotinonitrile-chromene) hybrids linked to pyrazole units as potential acetylcholinesterase inhibitors
Sherif M. H. Sanad, Ahmed E. M. Mekky
Synthetic Communications (2022) Vol. 52, Iss. 16, pp. 1672-1684
Closed Access | Times Cited: 8
Sherif M. H. Sanad, Ahmed E. M. Mekky
Synthetic Communications (2022) Vol. 52, Iss. 16, pp. 1672-1684
Closed Access | Times Cited: 8
Tandem synthesis, cytotoxicity, and in silico study of new 1,3,4‐oxadiazoles as potential thymidylate synthase inhibitors
Sherif M. H. Sanad, Ahmed E. M. Mekky, Ahmed A. M. Ahmed
Archiv der Pharmazie (2022) Vol. 355, Iss. 10
Closed Access | Times Cited: 7
Sherif M. H. Sanad, Ahmed E. M. Mekky, Ahmed A. M. Ahmed
Archiv der Pharmazie (2022) Vol. 355, Iss. 10
Closed Access | Times Cited: 7
New bis(thieno[2,3-b]pyridine) hybrids linked to arene units as potential bacterial biofilm and MRSA inhibitors
Sherif M. H. Sanad, Ahmed E. M. Mekky
Canadian Journal of Chemistry (2023) Vol. 101, Iss. 8, pp. 538-547
Closed Access | Times Cited: 3
Sherif M. H. Sanad, Ahmed E. M. Mekky
Canadian Journal of Chemistry (2023) Vol. 101, Iss. 8, pp. 538-547
Closed Access | Times Cited: 3
Synthesis of Phosphonylated 5-Alkyl-1,3,4-oxadiazoles Based on Dialkyl Chloroethynylphosphonates
Е. А. Герасимова, D. M. Egorov
Russian Journal of General Chemistry (2024) Vol. 94, Iss. 8, pp. 1941-1954
Closed Access
Е. А. Герасимова, D. M. Egorov
Russian Journal of General Chemistry (2024) Vol. 94, Iss. 8, pp. 1941-1954
Closed Access
Design, Synthesis, and Biological Evaluation of 2-Butyl-4-Chloroimidazole-Derived 1,3,4-Oxadiazoles: ACE Inhibition, Anticancer, and Antitubercular Activities
R. Manjunath, Preethi G. Anantharaju, Subbarao V Madhunapantulas, et al.
Journal of Molecular Structure (2024) Vol. 1322, pp. 140630-140630
Open Access
R. Manjunath, Preethi G. Anantharaju, Subbarao V Madhunapantulas, et al.
Journal of Molecular Structure (2024) Vol. 1322, pp. 140630-140630
Open Access
Microwave-assisted synthesis of nicotinonitrile and/or arene-linked bis(chromene-thiazoles) as new VRE and MRSA inhibitors
Ahmed E. M. Mekky, Sherif M. H. Sanad
Synthetic Communications (2022) Vol. 52, Iss. 24, pp. 2276-2290
Closed Access | Times Cited: 3
Ahmed E. M. Mekky, Sherif M. H. Sanad
Synthetic Communications (2022) Vol. 52, Iss. 24, pp. 2276-2290
Closed Access | Times Cited: 3
Syntheses and Antioxidant Activity of 1-Isonicotinoyl-4-phenylthiosemicarbazide and Crystal Structures of N-Phenyl-5-(pyridin-4-yl)-1,3,4-oxadiazol-2-amine Hydrochloride and 4-Phenyl-3-(pyridin-4-yl)-1H-1,2,4-triazole-5(4H)-thione derived from 1 Isonicotinoyl-4-phenylthiosemicarbazide
Ndama Faye, Bédié Mbow, Aïssatou Alioune Gaye, et al.
Earthline Journal of Chemical Sciences (2022), pp. 189-208
Open Access | Times Cited: 3
Ndama Faye, Bédié Mbow, Aïssatou Alioune Gaye, et al.
Earthline Journal of Chemical Sciences (2022), pp. 189-208
Open Access | Times Cited: 3
NOVEL SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL ACTIVITY OF N-(5BROMO-2-(5-PHENYL1,3,4-OXADIAZOL-2-YL)NAPHTHA[2,1-B]FURAN-1- YL)ACETAMIDE AND N-(5-NITRO-2-(5-PHENYL-1,3,4- OXADIAZOL-2-YL)NAPHTHA[2,1-BFURAN-1-YL]ACETAMIDE AND THEIR DERIVATIVES
K. M. Nagarsha, T. M. Sharanakumar, D. Ramesh, et al.
RASAYAN Journal of Chemistry (2023) Vol. 16, Iss. 01, pp. 167-175
Open Access
K. M. Nagarsha, T. M. Sharanakumar, D. Ramesh, et al.
RASAYAN Journal of Chemistry (2023) Vol. 16, Iss. 01, pp. 167-175
Open Access
DESIGN, SYNTHESIS, MOLECULAR DOCKING, AND ANTIMICROBIAL STUDY ON NAPHTHOFURAN DERIVATIVES
S. Raghavendra, M. N. Kumaraswamy, K. M. Nagarsha, et al.
RASAYAN Journal of Chemistry (2023) Vol. 16, Iss. 03, pp. 1613-1623
Open Access
S. Raghavendra, M. N. Kumaraswamy, K. M. Nagarsha, et al.
RASAYAN Journal of Chemistry (2023) Vol. 16, Iss. 03, pp. 1613-1623
Open Access
A Review of Modern Methods of Synthesis 1, 3, 4-Oxadiazole as a Bioactive Compounds
Hajar Adeeb
Wasit Journal of Pure sciences (2023) Vol. 2, Iss. 4, pp. 237-253
Open Access
Hajar Adeeb
Wasit Journal of Pure sciences (2023) Vol. 2, Iss. 4, pp. 237-253
Open Access
