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Sort articles by: Volume | Date | Most Rates | Most Views | Reviews | Alphabet
1.

Solid state synthesis, characterization and biological evaluation of silver doped nanosized metal oxides Pages 821-830 Right click to download the paper Download PDF

Authors: G. Tanuja, Sangappa K Ganiger, Shashidhar Shashidhar, R.K. Preeti, Somanath Reddy Patil, Arunkumar Lagashetty

DOI: 10.5267/j.ccl.2023.3.011

Keywords: Pyrazolo[3, 4-d]pyrimidine, Thiazolo[3, 2-a]pyrimidine, Antibacterial activity, Antifungal activity, Heterocycles

Abstract:
Nanomaterials have attracted a great deal of attention from the scientific community due to their unique properties and applications. The small size metal oxides have opened up the door for intensive research to utilize their properties for biomedical applications. Silver nanoparticle (AgNPs) and metal oxide nanomaterials like MgO, ZnO, NiO and its silver doped nanocomposites (Ag-MgO, Ag-ZnO, Ag-NiO) have been prepared using solid state combustion method using polyvinyl alcohol (PVA) as a fuel. The structure of as prepared oxides and its silver doped nanocomposites were characterized using X-ray diffraction (XRD) tool and morphology by Scanning Electron Micrograph (SEM) tool as well as Transmission electron micrograph tool respectively. Presence of the metals in the oxides and its Ag composite was confirmed by the EDX pattern. Bonding nature in the composite is well studied by the Fourier transform infrared (FT-IR) tool. Antibacterial activity studies of the nanocomposites are carried out against various bacteria.
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Journal: CCL | Year: 2023 | Volume: 12 | Issue: 4 | Views: 912 | Reviews: 0

 
2.

Synthesis, characterization and biological study of some new substituted pyrazolo[3,4-d] thiazolo[3,2-a] pyrimidine derivatives Pages 831-838 Right click to download the paper Download PDF

Authors: Mukesh M. Chavda, Manoj F. Dhaduk, Jatin M. Upadhyay

DOI: 10.5267/j.ccl.2023.3.010

Keywords: Pyrazolo[3, 4-d]pyrimidine, Thiazolo[3, 2-a]pyrimidine, Antibacterial activity, Antifungal activity, Heterocycles

Abstract:
Fused pyrimidines play an imperative role in our life due to their biological importance in the struggle of microorganisms. A series of 4-aryl-3-methyl-1-phenyl-1,4,6,7-tetrahydropyrazolo[3,4-d] thiazolo[3,2-a]pyrimidine (4a-j) were synthesized by cyclization of 3-methyl-1-phenyl-4-aryl-1,4,5,7-tetrahydro-6H-pyrazolo[3,4-d]pyrimidine-6-thiones (3a-j) with 1,2-dibromoethane in presence of anhydrous potassium carbonate. Earlier, compounds (3a-j) were synthesized by the condensation of 5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one (2), different substituted benzaldehyde and thiourea with catalytic amount of con. HCl in methanol. Compound 2 was synthesized by condensation of ethyl acetoacetate (1) and phenylhydrezine in presence of a catalytic amount of acetic acid at reflux temperature. The constitution of the synthesized products has been characterized by using elemental analysis, Infrared, 1H-NMR spectroscopy and further supported by Mass spectroscopy. All the products have been screened for their in-vitro biological assay like antibacterial and antifungal activity at concentration of 500 μg/ml. It was exposed that most of the compounds displayed inspiring antibacterial and antifungal activity compared to the used reference standard.
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Journal: CCL | Year: 2023 | Volume: 12 | Issue: 4 | Views: 951 | Reviews: 0

 
3.

Synthesis of fused heterocycles from 2-aryl-5-(chlorosulfonyl)-1,3-oxazole-4-carboxylates and α-aminoazoles involving the Smiles rearrangement Pages 101-110 Right click to download the paper Download PDF

Authors: Maryna Kachaeva, Stepan Pilyo, Sergiy Popilnichenko, Andrii Kornienko, Eduard Rusanov, Volodymyr Prokopenko, Vladimir Zyabrev, Volodymyr S. Brovarets

DOI: 10.5267/j.ccl.2018.9.001

Keywords: 1, 3-Oxazole-5-sulfonyl chloride, Aminoazole, Smiles rearrangement, [1, 3]Oxazolo[5, 4-d]pyrimidine

Abstract:
Reaction of methyl 2-aryl-5-(chlorosulfonyl)-1,3-oxazole-4-carboxylates with 1H-pyrazol-5-amines and 1H-1,2,4-triazol-5-amines proceeds with the participation of endocyclic aminoazole nitrogen atoms to yield products containing a primary amino group. Being treated by sodium hydride these products undergo a further transformation into the tricyclic compounds. It has been shown that the cyclocondensation pathway includes the Smiles rearrangement with extrusion of SO2 followed by the elimination of MeOH. This reaction sequence is a convenient approach to the synthesis of new annulated [1,3]oxazolo[5,4-d]pyrimidine derivatives.
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Journal: CCL | Year: 2018 | Volume: 7 | Issue: 4 | Views: 1895 | Reviews: 0

 

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