Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Ivan Hameed R. Tomi"'
Autor:
Ivan Hameed R. Tomi, Ali Hussein R. Al-Daraji, Raya Raad T. Al-Qaysi, Mohammed Mujbel Hasson, Khlood Hamed D. Al-Dulaimy
Publikováno v:
Arabian Journal of Chemistry, Vol 7, Iss 5, Pp 687-694 (2014)
In this study we synthesized the new compounds containing bis-1,3,4-thiadiazole 3(A–D)n from many reaction steps (cyclization, diazotization and etherification respectively). The compounds have been characterized by melting point, FT-IR and 1H NMR
Externí odkaz:
https://doaj.org/article/2b021cf4dbca424da6f13ef189375f84
Publikováno v:
E-Journal of Chemistry, Vol 9, Iss 2, Pp 962-969 (2012)
In this study, two new Schiff base compounds derived from the condensation reaction of L-glycine and L-tryptophan with 4-methylbenzal-dehyde have been synthesized. The Schiff base compounds were characterized by FT-IR, UV and 1H NMR spectroscopy. The
Externí odkaz:
https://doaj.org/article/0f973756fa68438081587de4ab8e2372
Autor:
Gassan Q. Ali, Gamal A. El-Hiti, Ivan Hameed R. Tomi, Raghad Haddad, Alaa J. Al-Qaisi, Emad Yousif
Publikováno v:
Molecules, Vol 21, Iss 12, p 1699 (2016)
Series of 4-(4-substituted benzylideneamino)-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazole-3-thiols were synthesized and their structures were confirmed. The synthesized Schiff bases were used as photostabilizers for polystyrene against photodegradati
Externí odkaz:
https://doaj.org/article/192d3380aab24013b8115941695cbfb2
Publikováno v:
Journal of Adhesion Science and Technology. 37:1525-1542
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a461c0ea6fed920bb5d40cc210930d4
https://doi.org/10.1080/01694243.2022.2086398
https://doi.org/10.1080/01694243.2022.2086398
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8c4690ee6448b454b082585aad6721b
https://doi.org/10.1002/slct.202200920
https://doi.org/10.1002/slct.202200920
Autor:
Ivan Hameed R. Tomi, Al-Ameen Bariz OmarAli, Ahmed Jasim M. Al-Karawi, Dhafir T. A. Al Heetimi
Publikováno v:
Molecular Crystals and Liquid Crystals. 722:8-26
2-(4-Alkoxyphenyl)-5-(p-tolyl)-1,3,4-thiadiazoles (alkoxy: O(CH2)nH, n = 1–8) (6a–h) (as a series of 1,3,4-thiadiazole derivatives) and their silver(I) complexes: bis(2-(4-alkoxyphenyl)-5-(p-tolyl)...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddc05833bd3369030a37517d8f0bd17d
https://doi.org/10.1080/15421406.2020.1860624
https://doi.org/10.1080/15421406.2020.1860624
Autor:
Ahmed H. Ismail, Ivan Hameed R. Tomi, Younis Baqi, Ali Hussein R. Al-Daraji, Ahmed Mutanabbi Abdula
Publikováno v:
Medicinal Chemistry. 17:462-473
Background: The frequent use of antibacterial agents leads to antimicrobial resistance, which is one of the biggest threats to global health today. Therefore, the discovery of novel antimicrobial agents is still urgently needed to overcome the severe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3dd6bfc7c82095b708b5799d4739e42
https://doi.org/10.2174/1573406415666191107121757
https://doi.org/10.2174/1573406415666191107121757
Publikováno v:
ChemistrySelect. 5:8740-8744
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a79e1f8a7c9c2140eb84af47373c283c
https://doi.org/10.1002/slct.202001857
https://doi.org/10.1002/slct.202001857
Publikováno v:
Chemical Papers. 74:1739-1757
An oxadiazole derivative 4-[3-(4-methylphenyl)-1,2,4-oxadiazol-5-yl]-phenol (MOP) has been investigated as a protector against corrosion of mild steel tanks in Iraqi kerosene reservoirs using the Tafel approach. The extrapolation study was carried ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97468b26b5b08a5a058e97ae6f7e3bd3
https://doi.org/10.1007/s11696-019-01022-2
https://doi.org/10.1007/s11696-019-01022-2
Publikováno v:
ChemistrySelect. 4:9883-9892
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a3c37241bd999605bd96199d74736bd
https://doi.org/10.1002/slct.201902398
https://doi.org/10.1002/slct.201902398