| Year |
Citation |
Score |
| 2023 |
Moussa Z, Paz AP, Khalaf MA, Judeh ZMA, Samadi A, Alzamly A, Al-Fahemi JH, Tatina MB, Al-Masri HT, Jassas RS, Ahmed SA. First Exclusive Stereo- and Regioselective Preparation of 5-Arylimino-1,3,4-Selenadiazole Derivatives: Synthesis, NMR analysis, and Computational Studies. Chemistry, An Asian Journal. e202300475. PMID 37495559 DOI: 10.1002/asia.202300475 |
0.321 |
|
| 2023 |
Moussa Z, Paz AP, Judeh ZMA, Alzamly A, Saadeh HA, Asghar BH, Alsaedi S, Masoud B, Almeqbaali S, Estwani S, Aljaberi A, Al-Rooqi MM, Ahmed SA. First X-ray Crystal Structure Characterization, Computational Studies, and Improved Synthetic Route to the Bioactive 5-Arylimino-1,3,4-thiadiazole Derivatives. International Journal of Molecular Sciences. 24. PMID 36835167 DOI: 10.3390/ijms24043759 |
0.301 |
|
| 2022 |
Moussa Z, Kaddoura R, Saadeh HA, Abutaha N, Ahmed SA. Highly bioactive novel aryl-, benzyl-, and piperazine-selenoureas: synthesis, structural characterization and in vitro biological evaluation. Heliyon. 8: e10709. PMID 36185149 DOI: 10.1016/j.heliyon.2022.e10709 |
0.302 |
|
| 2022 |
Moussa Z, Judeh ZMA, Alzamly A, Ahmed SA, Tomah Al-Masri H, Al-Hindawi B, Rasool F, Saada S. Iodine-DMSO mediated conversion of -arylcyanothioformamides to -arylcyanoformamides and the unexpected formation of 2-cyanobenzothiazoles. Rsc Advances. 12: 6133-6148. PMID 35424574 DOI: 10.1039/d2ra00049k |
0.3 |
|
| 2021 |
Alsharif MA, Raja QA, Majeed NA, Jassas RS, Alsimaree AA, Sadiq A, Naeem N, Mughal EU, Alsantali RI, Moussa Z, Ahmed SA. DDQ as a versatile and easily recyclable oxidant: a systematic review. Rsc Advances. 11: 29826-29858. PMID 35479576 DOI: 10.1039/d1ra04575j |
0.313 |
|
| 2021 |
Wati FA, Santoso M, Moussa Z, Fatmawati S, Fadlan A, Judeh ZMA. Chemistry of trisindolines: natural occurrence, synthesis and bioactivity. Rsc Advances. 11: 25381-25421. PMID 35478918 DOI: 10.1039/d1ra03091d |
0.389 |
|
| 2020 |
Moussa Z, Al-Mamary M, Al-Juhani S, Ahmed SA. Preparation and biological assessment of some aromatic hydrazones derived from hydrazides of phenolic acids and aromatic aldehydes. Heliyon. 6: e05019. PMID 33024857 DOI: 10.1016/j.heliyon.2020.e05019 |
0.352 |
|
| 2016 |
Moussa Z, El-Sharief MA, Abbas SY. New imidazolidineiminothione derivatives: Synthesis, spectral characterization and evaluation of antitumor, antiviral, antibacterial and antifungal activities. European Journal of Medicinal Chemistry. 122: 419-428. PMID 27393950 DOI: 10.1016/J.Ejmech.2016.06.051 |
0.377 |
|
| 2011 |
Kong K, Moussa Z, Lee C, Romo D. Total synthesis of the spirocyclic imine marine toxin (-)-gymnodimine and an unnatural C4-epimer. Journal of the American Chemical Society. 133: 19844-56. PMID 22023219 DOI: 10.1021/Ja207385Y |
0.439 |
|
| 2011 |
El-Sharief MAMS, Moussa Z, El-Sharief AMS. Synthesis, characterization, and derivatization of some novel types of fluorinated mono- and bis-imidazolidineiminothiones with antitumor, antiviral, antibacterial, and antifungal activities Journal of Fluorine Chemistry. 132: 596-611. DOI: 10.1016/J.Jfluchem.2011.06.015 |
0.309 |
|
| 2009 |
El-Sharief AM, Moussa Z. Synthesis, characterization and derivatization of some novel types of mono- and bis-imidazolidineiminothiones and imidazolidineiminodithiones with antitumor, antiviral, antibacterial and antifungal activities--part I. European Journal of Medicinal Chemistry. 44: 4315-34. PMID 19664865 DOI: 10.1016/j.ejmech.2009.07.019 |
0.369 |
|
| 2006 |
Moussa Z, Romo D. Mild deprotection of primary N-(p-toluenesulfonyl) amides with SmI 2 following trifluoroacetylation Synlett. 3294-3298. DOI: 10.1055/S-2006-951530 |
0.311 |
|
| 2005 |
Kong K, Moussa Z, Romo D. Studies toward a marine toxin immunogen: enantioselective synthesis of the spirocyclic imine of (-)-gymnodimine. Organic Letters. 7: 5127-30. PMID 16268519 DOI: 10.1021/Ol051840R |
0.438 |
|
| 2005 |
Back TG, Moussa Z. Mimetics of the Selenoenzyme Glutathione Peroxidase: Novel Structures and Unusual Catalytic Mechanisms Phosphorus, Sulfur, and Silicon and the Related Elements. 180: 767-776. DOI: 10.1080/10426500590906238 |
0.607 |
|
| 2004 |
Back TG, Moussa Z, Parvez M. The exceptional glutathione peroxidase-like activity of di(3-hydroxypropyl) selenide and the unexpected role of a novel spirodioxaselenanonane intermediate in the catalytic cycle. Angewandte Chemie (International Ed. in English). 43: 1268-70. PMID 14991795 DOI: 10.1002/Anie.200353128 |
0.548 |
|
| 2004 |
Back TG, Moussa Z, Parvez M. PREPARATION AND X-RAY CRYSTAL STRUCTURES OF TWO ALIPHATIC SELENENYL BROMIDES STABILIZED BY N─SE COORDINATION Phosphorus, Sulfur, and Silicon and the Related Elements. 179: 2569-2579. DOI: 10.1080/10426500490494543 |
0.535 |
|
| 2003 |
Back TG, Moussa Z. Diselenides and allyl selenides as glutathione peroxidase mimetics. Remarkable activity of cyclic seleninates produced in situ by the oxidation of allyl omega-hydroxyalkyl selenides. Journal of the American Chemical Society. 125: 13455-60. PMID 14583041 DOI: 10.1021/Ja0357588 |
0.606 |
|
| 2002 |
Back TG, Moussa Z. Remarkable activity of a novel cyclic seleninate ester as a glutathione peroxidase mimetic and its facile in situ generation from allyl 3-hydroxypropyl selenide. Journal of the American Chemical Society. 124: 12104-5. PMID 12371844 DOI: 10.1021/Ja028030K |
0.602 |
|
| 2002 |
Back TG, Moussa Z, Parvez M. Asymmetric methoxyselenenylations and cyclizations with 3-camphorseleno electrophiles containing oxime substituents at C-2. Formation of an unusual oxaselenazole from an oxime-substituted selenenyl bromide. The Journal of Organic Chemistry. 67: 499-509. PMID 11798323 DOI: 10.1021/Jo016061C |
0.563 |
|
| 2001 |
Back TG, Moussa Z. ChemInform Abstract: New Chiral Auxiliaries for Highly Stereoselective Asymmetric Methoxyselenenylations. Cheminform. 32: no-no. DOI: 10.1002/chin.200101055 |
0.516 |
|
| 2000 |
Back TG, Moussa Z. New chiral auxiliaries for highly stereoselective asymmetric methoxyselenenylations. Organic Letters. 2: 3007-9. PMID 10986094 DOI: 10.1021/Ol000187Z |
0.572 |
|
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