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Wyszukujesz frazę "Patel, P. K." wg kryterium: Autor


Tytuł:
Synthesis and characterization of novel 2-oxo-4-((4-(3-oxomorpholino)phenyl)amino)-2H-chromene-3-carbonitrile derivatives
Autorzy:
Jilariya, Krushnakumar J.
Chodvadiya, Vijay D.
Patel, P. K.
Babariya, Jayesh
Tematy:
3-cyano-4chlor coumarin
4-(4-aminophenyl)morpholin-3-one
antimicrobial activity
Pokaż więcej
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Powiązania:
https://bibliotekanauki.pl/articles/1075711.pdf  Link otwiera się w nowym oknie
Opis:
A highly functionalized heterocyclic library were synthesized, and characterized by common spectroscopic methods. This novel synthetic rout involves nucleophilic substitution reaction of 3-cyano-4chloro coumarin with 4-(4-aminophenyl)morpholin-3-one in the presence of base and methanol as a solvent in good yield and high purity. Key starting material 4-(4-aminophenyl)morpholin-3-one synthesized from aniline. The reaction of aniline with ethylene oxide gives INT-1 which on reaction with Chloroacetyl chloride yield INT-b. Nitration of INT-b gives INT-c, which on reduction with Sn/HCl gives int-D. Further INT-3 was synthesized from 4-hydroxy coumarin. The Vilsmeier-haack reaction of 4-hydroxy coumarin gives INT-01 which on reaction with hydroxylamine hydrochloride and sodium acetate furnished INT-03. All the synthesized compound of libraries characterized using 1H NMR, Mass, and IR spectroscopic technique.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis and characterization of novel 2-oxo-4-((4-(3-oxomorpholino)phenyl)amino)-2H-chromene-3-carbaldehyde derivatives
Autorzy:
Jilariya, Krushnakumar J.
Sanghani, Yogesh J.
Patel, P. K.
Babariya, Jayesh
Tematy:
4-(4-aminophenyl)morpholin-3-one
4-chloro-2-oxo-2H-chromene-3-carbaldehyde
antimicrobial activity
Pokaż więcej
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Powiązania:
https://bibliotekanauki.pl/articles/1068631.pdf  Link otwiera się w nowym oknie
Opis:
A highly functionalized heterocyclic library were synthesized, characterized and tested for biological evaluation against bacteria and fungus. This novel synthetic rout involves nucleophilic substitution reaction of 4-chloro-2-oxo-2H-chromene-3-carbaldehyde with 4-(4-aminophenyl) morpholin-3-one in the presence of base and methanol as a solvent in good yield and high purity. All the synthesized compound of libraries characterized using 1H NMR, Mass, and IR spectroscopic technique. Also all compound screened for antimicrobial activity against standard drugs.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis and Characterization of N-Methyl Indole Derivatives via Desulfitative Displacement by Various Amines and Its Antimicrobial Activity
Autorzy:
Chodvadiya, Vijay D.
Pambhar, Kaushik D.
Parmar, Nilesh D.
Dhamsaniya, Ashish P.
Safi, Shahrukh khan A.
Chhatbar, Pratiksha V.
Ram, Hemal N.
Khunt, Ranjan C.
Patel, P. K.
Tematy:
Anti-microbial agents
Desulfitative displacement
N-methyl indole
S-methyl
Pokaż więcej
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Powiązania:
https://bibliotekanauki.pl/articles/1065130.pdf  Link otwiera się w nowym oknie
Opis:
A modular three step synthetic approach of N-methyl indole derivatives has been carried out by the condensation of N-methyl indole with cyanoacetic acid using acetic anhydride as solvent to yield 3-cyanoacetyl N-methyl indole, which further reacts with carbon disulphide and methyl iodide in basic condition to obtain 2-(1-methyl-1H-indole-3-carbonyl)-3,3-bis(methylthio)acrylonitrile as a scaffold. Subsequent, the scaffold when reacts with substituted various amine derivatives via desulfitative displacement forms new derivatives of 3-((substitutedphenyl)amino)-2-(1-methyl-1H-indole-3-carbonyl)-3-(methylthio)acrylonitrile in moderate to good yields. All the novel compounds were evaluated for their antimicrobial activity against Gram+ve and Gram-ve bacteria and different fungal species which demonstrated well to moderate antimicrobial activity.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
On Phonon Dispersion in Alkali Metals
Autorzy:
Gajjar, P. N.
Thakore, B. Y.
Patel, H. K.
Jani, A. R.
Tematy:
71.25.Cx
63.20.Dj
Pokaż więcej
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Powiązania:
https://bibliotekanauki.pl/articles/1933617.pdf  Link otwiera się w nowym oknie
Opis:
In the present paper, the calculation of the phonon dispersion relations for alkali metals to second order in a local pseudopotential is discussed in terms of the real-space sum. Different forms of dielectric functions are employed to judge the varying effects of exchange and correlation on the phonon frequencies. The quantitative agreement of phonon frequencies for the alkali metals reflects, satisfactorily, the experimental trend.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis and in vitro antibacterial and antifungal evaluation of quinoline analogue azetidin and thiazolidin derivatives
Autorzy:
Prajapati, S. M
Vekariya, R. H.
Patel, K. D.
Panchal, S. N.
Patel, H. D.
Rajani, D. P.
Rajani, S.
Tematy:
antibacterial
antifungal
quinoline
azetidin derivatives
thiazolidin derivatives
Pokaż więcej
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Powiązania:
https://bibliotekanauki.pl/articles/412324.pdf  Link otwiera się w nowym oknie
Opis:
A library of quinoline analog two novel series of azetidin (SH1-5) and thiazolidin (SHa-e) derivatives were designed and synthesized with simple and eco-friendly methodologies. The structures of the compounds were elucidated with the aid of elemental analysis, IR, 1H-NMR and mass spectral data. These novel synthesized compounds were evaluated for antibacterial activity against two gram-positive bacteria (Staphylococcus aureus, Staphylococcus pyogenus) and two gram-negative bacteria (Pseudomonas aeruginosa, Escherichia coli). The title compounds were also studied for their antifungal activity with Candida albicans, Aspergillus niger, Aspergillus clavatus using the broth dilution technique. Most of the compounds were the best bio-active desired antibacterial analog with less MIC value against different tested strains.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Bioremediation of melanoidin contamination in distillery effluent using Aspergillus brasiliensis
Autorzy:
Singh, T.A.
Singh, T.
Singh, R.
Pandey, P.K.
Gaur, R.
Jamal, F.
Patel, S.K.
Bansal, S.
Tematy:
spent wash
effluent
melanoidin
bioremediation
decolorization
Pokaż więcej
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Powiązania:
https://bibliotekanauki.pl/articles/2097092.pdf  Link otwiera się w nowym oknie
Opis:
The current investigation is the first report of utilization of Aspergillus brasiliensis for the decolorization of melanoidin in distillery effluent. The effluent generated from alcohol distilleries is one of the most complex wastewater with a high biological oxygen demand (BOD) and other organic, inorganic, and toxic constituents. The effluent contains melanoidin, a dark brown compound, which is difficult to remediate by using conventional technologies. The disposal of spent wash in the natural environment is hazardous and can deteriorate land and water resources. The decolorization of spent wash through physical and chemical methods remains unsuitable, and the only alternative to decolorize spent wash is biological treatment. In the current study, three fungal strains were isolated from the distillery waste and screened for their ability to decolorize melanoidin.The isolate RS2 exhibited maximum decolorization of 83% and was identified as Aspergillus brasiliensis. Its optimum growth temperature was 37EC, and the maximum efficiency was recorded after 120 h of incubation. Nutritional sources were investigated for the fungi showing the maximum decolorization of melanoidin, and starch and peptone were found to be the best carbon and nitrogen sources, respectively. At 1.5% starch concentration and 1.5% peptone concentration, the decolorization level attained was 87.45% and 88.74%, respectively. A. brasiliensis exhibited a high potential to decolorize melanoidin. The decolorization percentage was high, which makes this fungus a potential candidate for use at the industrial scale for the bioremediation of spent wash.
Dostawca treści:
Biblioteka Nauki
Artykuł

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