Zobrazeno 1 - 10 of 11 pro vyhledávání: '"Somayeh Ghazi"'
1
Akademický článek
An efficient ultrasonic-assisted synthesis of ethyl-5-(aryl)-2-(2-alkokxy-2-oxoethylidene)-7-methyl-3-oxo-3, 5-dihydro-2H-thiazolo [3, 2-a] pyrimidine-6-carboxylate derivatives
Autor: Ali Darehkordi, Somayeh Ghazi
Publikováno v: Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2175-2182 (2019)
Dihydropyrimidinone derivatives were prepared by tri-component reaction of ethyl aceto acetate, aldehydes and thiourea in the presence of modified montmorillonite nanostructure as a catalyst and used as key intermediates for the synthesis of ethyl-5-
Externí odkaz: https://doaj.org/article/bb0123e6c653442983ab74be8dac0463
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2
Akademický článek
Synthesis of a New Class of Tris- and Bis(1,3,4-thiadiazol-2-amine) Methyl and Ethyl Tris- and Bis-2-(2-(2-benzoyl hydrazinyl)-4-oxothiazolidine) Acetate Derivatives
Autor: Ali Darehkordi, Somayeh Ghazi
Publikováno v: Journal of Chemistry, Vol 2013 (2013)
Hydrazine, carbothioamide derivatives 2, 3, and 4 were synthesized by the condensation of 1, 3, 5-tri carbonyl tri chloride, Terephthaloyl dichloride, and 1, 4-dicarbonyl chloride with thiosemicarbazide in presence of pyridine as a solvent. The react
Externí odkaz: https://doaj.org/article/c058beb4d18044d4bf518675e049c956
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4
Type II c-Met inhibitors: molecular insight into crucial interactions for effective inhibition
Autor: Tahereh Damghani, Somayeh Pirhadi, Zahra Haghighijoo, Maryam Elyasi, Somayeh Ghazi
Publikováno v: Molecular diversity. 26(3)
The c-Met tyrosine kinase plays an important role in human cancers. Preclinical studies demonstrated that c-Met is over-expressed, mutated and amplified in a variety of human tumor types and design of more potent c-Met inhibitors is a priority. In th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75020c1854cc1da66d4dde3e20bf9624
https://pubmed.ncbi.nlm.nih.gov/34247323
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5
Urease Enzyme Inhibitory of Heavy Metals and Organic Solvents in Ammonia Making for Synthesis of Nifedipine Antihypertensive Drug
Autor: Fatemah Tamaddon, Mohammad Reza Noorbala, Davood Arab, Somayeh Ghazi
Publikováno v: Toloo-e-behdasht, Vol 17, Iss 1, Pp 96-104 (2018)
Introduction: Simultaneous development of technology is composed with environmental hazardous with heavy-metals and organic solvents and thus toxic catalysts/organic solvents must be replaced with biocatalysts and water. Urease is a hydrolase enzyme
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doajarticles::0bd5495c5dd498a9fb48cb0c71f3a674
http://tbj.ssu.ac.ir/browse.php?a_code=A-10-1948-1&slc_lang=en&sid=1
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6
Urease-catalyzed synthesis of aminocyanopyridines from urea under fully green conditions
Autor: Mohammad R. Noorbala, Somayeh Ghazi, Fatemeh Tamaddon
Publikováno v: Journal of Molecular Catalysis B: Enzymatic. 127:89-92
This is an original work on catalytic performance of urease in organic synthesis which in one-pot dissociation of urea and condensation of the in situ generated ammonia with aldehydes, acetophenones, and malononitrile occurs in water to give 2-amino-
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a84e47562c1313ca618e5d0713d315cf
https://doi.org/10.1016/j.molcatb.2016.02.015
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7
Urease: A highly biocompatible catalyst for switchable Biginelli reaction and synthesis of 1,4-dihydropyridines from the in situ formed ammonia
Autor: Fatemeh Tamaddon, Somayeh Ghazi
Publikováno v: Catalysis Communications. 72:63-67
Urease is a superior biocompatible catalyst for switching from the Biginelli reaction to urea-based synthesis of 1,4-dihydropyridines in water, where 100% switching occurs at 0.02 g/mL of enzyme. Hantzsch reaction with ammonium acetate (NH 4 OAc) is
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9f600acd75ef0467351969abf1209b66
https://doi.org/10.1016/j.catcom.2015.09.006
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8
Synthesis of N-aryl-2,2,2-trifluoroacetimidoyl piperazinylquinolone derivatives and their antibacterial evaluations
Autor: Mahmood Javanmiri, Ali Darehkordi, Somayeh Ghazi, Shokrollah Assar
Publikováno v: Journal of Fluorine Chemistry. 132:263-268
N -substituted trifluoroacetimidoyl chlorides were used for the synthesis of new piperazinylquinolone derivatives. These reactions provided N -aryl-2,2,2-trifluoroacetimidoyl piperazinylquinolone derivatives in good yields. Two selected compounds wer
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d38c9504f9e2b08c4299d94fc8072c5b
https://doi.org/10.1016/j.jfluchem.2011.02.002
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9
An efficient ultrasonic-assisted synthesis of ethyl-5-(aryl)-2-(2-alkokxy-2-oxoethylidene)-7-methyl-3-oxo-3, 5-dihydro-2H-thiazolo [3, 2-a] pyrimidine-6-carboxylate derivatives
Autor: Somayeh Ghazi, Ali Darehkordi
Publikováno v: Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2175-2182 (2019)
Dihydropyrimidinone derivatives were prepared by tri-component reaction of ethyl aceto acetate, aldehydes and thiourea in the presence of modified montmorillonite nanostructure as a catalyst and used as key intermediates for the synthesis of ethyl-5-
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef651bda28a6e18c24831a6cc564266d
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10
Synthesis of a New Class of Tris- and Bis(1,3,4-thiadiazol-2-amine) Methyl and Ethyl Tris- and Bis-2-(2-(2-benzoyl hydrazinyl)-4-oxothiazolidine) Acetate Derivatives
Autor: Somayeh Ghazi, Ali Darehkordi
Publikováno v: Journal of Chemistry, Vol 2013 (2013)
Hydrazine, carbothioamide derivatives2,3, and4were synthesized by the condensation of 1, 3, 5-tri carbonyl tri chloride, Terephthaloyl dichloride, and 1, 4-dicarbonyl chloride with thiosemicarbazide in presence of pyridine as a solvent. The reaction
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c8558c7074f9a185b5ce9152bc7e784
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