نتایج جستجو برای: 4 dihydropyrimidin 21h onesthiones

تعداد نتایج: 1303795  

2010
Hssain Bih Lahcen Bih Bouchaid Manoun Mohamed Azrour Peter Lazor Lahcen El Ammari

The title compound, (NH(4))(5)Na(7)[Mo(5)P(2)O(23)](2)·21H(2)O, was prepared under atmospheric conditions in aqueous solution at room temperature. The structure contains the [Mo(5)P(2)O(23)](6-) heteropolyoxometallate anion, which has been previously reported a number of times with a variety of differing counter-cations. Each anion is built up of five MoO(6) octa-hedra sharing an edge and formi...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2005
ahmad shaabani ayoob bazgir sakineh arab ameri masoumeh sharifi kiasaraie sima samadi

alkali and alkaline earth metals hydrogen sulfate catalyzed the one-pot three component condensation reactions of aldehydes, 1,3-dicarbonyl compounds and urea or thiourea under solvent-free conditions leading to 3,4-dihydropyrimidin-2(1h)-ones in high yields at 80 °c. our results showed that biginelli reaction not only is ph dependent, but the cation of catalyst plays an important role.

Journal: :international journal of heterocyclic chemistry 0
ali ezabadi central tehran branch, islamic azad university, sanat square, tehran, iran neda ghassemi central tehran branch, islamic azad university, sanat square, tehran, iran

d-tartaric acid is successfully used as a green and efficient catalyst for the synthesis of 3,4-dihydropyrimidin-2(1h)-ones under solvent-free conditions. the developed method has many advantages, including devoid of harmful catalyst and solvents, high yield and easily work-up.

Journal: :Anticancer research 2013
Agnieszka Gnyszka Zenon Jastrzebski Sylwia Flis

The DNA methyltransferase (DNMT) inhibitors azacytidine and decitabine are the most successful epigenetic drugs to date and are still the most widely used as epigenetic modulators, even though their application for oncological diseases is restricted by their relative toxicity and poor chemical stability. Zebularine (1-(β-D-ribofuranosyl)-1,2-dihydropyrimidin-2-one), a more stable and less toxic...

2017
Andreas C Boukis Baptiste Monney Michael A R Meier

The Biginelli reaction was combined with the Passerini reaction for the first time in a sequential multicomponent tandem reaction approach. After evaluation of all possible linker components and a suitable solvent system, highly functionalized dihydropyrimidone-α-acyloxycarboxamide compounds were obtained in good to excellent yields. In a first reaction step, different 3,4-dihydropyrimidin-2(1H...

2015
Chelsea den Hollander Jasper Visser Ellen de Haas Luca Incrocci Threes Smijs

Onychomycosis is predominantly caused by the dermatophytes Trichophyton rubrum, Trichophyton mentagrophytes and Trichophyton tonsurans. The main treatment obstacle concerns low nail-plate drug permeability. In vitro antifungal photodynamic treatment (PDT) and nail penetration enhancing effectiveness have been proven for multifunctional photosensitizer 5,10,15-tris(4-N-methylpyridinium)-20-(4-(b...

Journal: :Medicinal chemistry (Shariqah (United Arab Emirates)) 2014
Venugopala K Narayanaswamy Raquel M Gleiser Raju K Chalannavar Bharti Odhav

Eight novel dihydropyrimidine analogs named DHPM1-DHPM8 was synthesized in their hydrochloride salt form using one pot synthesis between methyl 2-chloro-4-(4-chlorophenyl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate and substituted arylamines in isopropanol. The antimosquito effect of the test compounds were assessed against the adult mosquito Anopheles arabiensis. For adulticidal properties t...

Journal: :Blood 2006
Michel Herranz Juan Martín-Caballero Mario F Fraga Jesús Ruiz-Cabello Juana Maria Flores Manuel Desco Victor Marquez Manel Esteller

Gene silencing by CpG island promoter hypermethylation has awakened the interest for DNA demethylating agents as chemotherapy drugs. Zebularine (1-[beta-D-ribofuranosil]-1,2-dihydropyrimidin-2-1) has been recently described as a new DNA methylation inhibitor. Here we have studied its effects in a mouse model of radiation-induced lymphomagenesis using nuclear magnetic resonance (NMR) and positro...

Journal: :iranian journal of catalysis 2013
jalal albadi azam mansournezhad

cuo-ceo2 nanocomposite is reported as a green and highly efficient recyclable catalyst for the multicomponent  synthesis of 3,4-dihydropyrimidin-2(1h)-ones/thiones under solvent-free conditions. the catalyst was synthesized by co-precipitation method and characterized by xrd, bet specific surface area, fesem and eds analysis.

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