Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Hanan Afifi"'
Autor:
Noha Hasaneen, Abdelaziz Ebead, Muhammad Murtaza Hassan, Hanan Afifi, Howard Hunter, Edward Lee-Ruff, Nadia S. El-Gohary, Azza R. Maarouf, Ali A. El-Emam
Publikováno v:
Molecules, Vol 24, Iss 18, p 3235 (2019)
The coupling of 2-bromo-3-benzoyloxycyclobutanone with purine under basic conditions produces two regioisomers consisting of the N-7 and N-9 alkylated products in equal amounts in their racemic forms. The distribution of the isomers is consistent wit
Externí odkaz:
https://doaj.org/article/4ff8ef9eff684a418eed543c88299e63
Autor:
Hanan Afifi, Alexandre Mikhailine, Gabriela Mladenova, Andrei Chtchemelinine, Israt Sultana, Tatiana Dyblenko, Evgeny Danilov, Rene Fournier, Edward Lee-Ruff
Publikováno v:
ARKIVOC, Vol 2012, Iss 6, Pp 343-354 (2012)
Externí odkaz:
https://doaj.org/article/4eec51550a194497a0f16c4fb4e23a5a
Autor:
Sohair Abd-El Mawgood Abd-ElMaksoud, Hala El-Bassyouni, Hanan Afifi, Manal Micheal Thomas, Alshaymaa Ahmed Ibrahim, Aliaa Shalaby, Tamer Ahmed Abdel Hamid, Nehal Abdel Hamid, Hany El-Ghobary
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 11, Pp SC17-SC20 (2015)
Introduction: Free radicals have been thought to participate in pathogenesis of peroxisomal disorders. Objective: The aim of the work is to detect free oxide radicals in blood of patients with peroxisomal disorders and to study their relation wit
Externí odkaz:
https://doaj.org/article/959779d4ec414080a7c0c80fe5d649f4
Publikováno v:
Molecules
Molecules, Vol 26, Iss 1069, p 1069 (2021)
Volume 26
Issue 4
Molecules, Vol 26, Iss 1069, p 1069 (2021)
Volume 26
Issue 4
Optimization of the extraction conditions of polyphenolic compounds for different parts of the Damas species, Conocarpus lancifolius and Conocarpus erectus, grown under UAE conditions was studied. The combination of ethanol concentration (50, 75, and
Autor:
Edward Lee-Ruff, Muhammad Murtaza Hassan, Hanan Afifi, Azza R. Maarouf, Nadia S. El-Gohary, Howard N. Hunter, Ali A. El-Emam, Noha Hasaneen, Abdelaziz Ebead
Publikováno v:
Molecules
Volume 24
Issue 18
Molecules, Vol 24, Iss 18, p 3235 (2019)
Volume 24
Issue 18
Molecules, Vol 24, Iss 18, p 3235 (2019)
The coupling of 2-bromo-3-benzoyloxycyclobutanone with purine under basic conditions produces two regioisomers consisting of the N-7 and N-9 alkylated products in equal amounts in their racemic forms. The distribution of the isomers is consistent wit
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 34:786-798
1-(2-Oxocyclobutyl-4-benzoyloxymethyl)-2,4(1H,3H)-pyrimidinedione and 1-(2-oxocyclobutyl-4-benzoyloxymethyl)-5-methyl-2,4(1H,3H)-pyrimidinedione can be prepared by reaction of uracil and thymine, respectively, with 3-benzoyloxymethyl-2-bromocyclobuta
Publikováno v:
Middle East Current Psychiatry. 21:95-105
Background Maladaptive behaviors and cognitive impairment in patients with Prader–Willi Syndrome can affect long-term functioning of patients and their family. Understanding difficulties underlying the maladaptive behavior allow better management.
Autor:
Ruhul Q. Chowdhury, Edward Lee-Ruff, Andrei Chtchemelinine, Hanan Afifi, Gabriela Mladenova, Tatiana Dyblenko, René Fournier, Alexander Enaya, A. B. P. Lever, Ryan Reiter
Publikováno v:
Photochemistry and Photobiology. 90:470-475
A series of 9-substituted fluorenols and 9,9'-disubstituted-9,9'-bifluorenyls were irradiated to give products derived from fluorenyl radicals. Product distribution was solvent dependent. A TEMPO adduct was isolated from the photoexcitation of 9-fluo
Autor:
Evgeny Danilov, Hanan Afifi, Alexandre Mikhailine, Edward Lee-Ruff, Israt Sultana, Gabriela Mladenova, Tatiana Dyblenko, Andrei Chtchemelinine, René Fournier
Publikováno v:
ARKIVOC, Vol 2012, Iss 6, Pp 343-354 (2012)
The 9-fluorenyl cation is a member of the 4N Huckel antiaromatic series of intermediates, first observed by time-resolved spectroscopy on UV photo-excitation of 9-fluorenol. [1] 9Trifluoromethyl-9-fluorenol incorporating an electron-withdrawing subst
Publikováno v:
Journal of Physical Organic Chemistry. 32:e3920