نتایج جستجو برای: 3 dihydroquinazolin 41h ones
تعداد نتایج: 1909670 فیلتر نتایج به سال:
In the present study, use of MgFe2O4@SiO2-SO3H as an efficient, green, magnetically recoverable & recyclable catalyst for micro-wave assisted solvent free synthesis 2,3-dihydroquinazolin-4(1H)-ones reaction pathway is presented. The superiorities this method are higher conversion rate, shorter time, easy isolation product and reusability without remarkable loss activity. synthesized derivatives...
A novel and mild Rh(III)-catalyzed [5+1] oxidative cycloaddition between arylguanidines and alkynes efficiently affords C4-disubstituted 1,4-dihydroquinazolin-2-amines. Members of this family of heterocycles, which contain the relevant cyclic guanidine units, have shown interesting pharmacological properties. The mechanism probably involves the formation of an eight-membered rhodacycle in which...
Herein we describe the synthesis and evaluation of a series of novel 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinazolin-1-ones for in vitro cytotoxicity against three human cancer cell lines as well as for potential antimalarial activity against the chloroquine-sensitive strain 3D7 of Plasmodium falciparum. The title compounds were prepared via PdCl₂-mediated endo-dig cyclization of 2-aryl-8-(arylethyn...
A bio-based magnetic nano-catalyst (Fe3O4@nano-dextrin/Ti(IV)) was synthesized via the preparation of Fe3O4@nano-dextrinas magnetic support and then its treatment with titanium tetrachloride (TiCl4). The properties of this catalyst were characterized by different kinds of techniques such as FT-IR, FESEM, TEM, ICP, XRF, VSM and TGA....
In the present work, we have planned a new magnetically recoverable nanocatalyst. The obtained nanocatalyst designated as Fe3O4@SiO2@DOPisatin-Ni (II) was characterized by FTIR, XRD, SEM, EDAX, VSM, AAS and TGA techniques. It was found that Fe3O4@SiO2@DOPisatin-Ni (II) successfully catalyses the synthesis of 2,3-dihydroquinazolin-4(1H)-ones, polyhydroquinoline and 5-substituted 1H-tetrazoles in...
The current study investigated the cytotoxic effect of 3-(5-chloro-2-hydroxybenzylideneamino)-2-(5-chloro-2-hydroxyphenyl)-2,3-dihydroquinazolin-41(H)-one (A) and 3-(5-nitro-2-hydroxybenzylideneamino)-2-(5-nitro-2-hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one (B) on MCF-7, MDA-MB-231, MCF-10A and WRL-68 cells. The mechanism involved in apoptosis was assessed to evaluate the possible pathways i...
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