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Akademický článek
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Autor:
Thaher, Bassam Abu, Al-Masri, Ihab, Wahedy, Kanan, Morjan, Rami, Aliwaini, Saeb, Al atter, Iman Mahmoud, Elmabhouh, Aayat Ahmed, ibwaini, Areej khaled AL, Alkhaldi, Saba Luay, Qeshta, Basem, Jacob, Claus, Deigner, Hans-Peter
Publikováno v:
Naunyn-Schmiedeberg's Archives of Pharmacology; Aug2023, Vol. 396 Issue 8, p1797-1810, 14p
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Wahedy, Kanan, Abu Thaher, Bassam A., Schollmeyer, Dieter, Almasri, Ihab, Morjan, Rami Y., Qeshta, Basem, Deigner, H-p
The side product of the cyclocondensation reaction between ethyl benzimidazole-2-carboxylate and the nitrile imine of the corresponding hydrazonyl chloride, C20H11BrClN5O, crystallized in two crystal forms. Form (1) is a co-crystal of the target comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4294::6ffd9184560ac0a5df2a222ad4477b1b
https://scripts.iucr.org/cgi-bin/paper?bt6995
https://scripts.iucr.org/cgi-bin/paper?bt6995
Autor:
Abu Thaher, Bassam A., Schollmeyer, Dieter, Qeshta, Basem, Wahedy, Kanan, Almasri, Ihab, Morjan, Rami Y., Deigner, H-p
In the title compound, C20H10Cl3N5O, the 13-membered ring system makes dihedral angles of 78.64 (9)° with the trichlorophenyl ring and 62.60 (10)° with the pyridine ring. The crystal packing is dominated by π–π interactions between the 13-membe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4294::9080cad2dbb1c77ee87c18509676af53
https://scripts.iucr.org/cgi-bin/paper?bt4030
https://scripts.iucr.org/cgi-bin/paper?bt4030
Autor:
Qeshta, Basem Salem Ateah
Reaction of hydrazonoyl chlorides 18a,b with picolines derivatives 86-89 The reaction of hydrazonoyl chloride 18a with picoline derivaties 86-89 in the presence of triethylamine gave the corresponding imidazo[1,2-a]pyridine 93-96. The reaction of hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4294::be6707e57165e58789cf1d8c95eb92ad
Autor:
Wahedy, Kanan, Thaher, Bassam Abu, Schollmeyer, Dieter, Almasri, Ihab, Morjan, Rami, Qeshta, Basem, Deigner, Hans-Peter
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications; Sep2017, Vol. 73 Issue 9, p1341-1343, 16p
Autor:
Abdel-Latif, Monzir S., Batniji, Amal, El-Agez, Taher M., Younis, Malak J., Ghamri, Hatem, Abu Thaher, Bassam A., Qeshta, Basem S., Abu-Awwad, Fakhr M., Taya, Sofyan A.
Publikováno v:
Journal of Nano- & Electronic Physics; 2016, Vol. 8 Issue 4, p1-9, 9p
Autor:
Wahedy K; Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Alazhar University-Gaza, Gaza Strip, Palestinian Territories., Abu Thaher B; Faculty of Science, Chemistry Department, Islamic University of Gaza Strip, Gaza Strip, Palestinian Territories., Schollmeyer D; Department of Organic Chemistry, Johannes Gutenberg-University Mainz, Duesbergweg 10-14, 55099 Mainz, Germany., Almasri I; Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Alazhar University-Gaza, Gaza Strip, Palestinian Territories., Morjan R; Faculty of Science, Chemistry Department, Islamic University of Gaza Strip, Gaza Strip, Palestinian Territories., Qeshta B; Faculty of Science, Chemistry Department, Islamic University of Gaza Strip, Gaza Strip, Palestinian Territories., Deigner HP; Hochschule Furtwangen (HFU), Fakultät Medical and Life Sciences, Jakob-Kienzle Strasse 17, 78054 Villingen-Schwenningen, Germany.; Fraunhofer IZI, EXIM Rostock, Perlickstrasse 1, 04103 Leipzig, Germany.
Publikováno v:
Acta crystallographica. Section E, Crystallographic communications [Acta Crystallogr E Crystallogr Commun] 2017 Aug 15; Vol. 73 (Pt 9), pp. 1341-1343. Date of Electronic Publication: 2017 Aug 15 (Print Publication: 2017).