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Sep 14, 2023Open Access
In this work, a new ligand (13)aneN4 with anthracene was synthesized and characterized by mass spectrometry, NMR, UV-Vis and fluorescence spectroscopies. The ligand has a double fluorescence explained by the presence of a photoinduced charge transfer. The fluorescence spectra in various solvents show an increase in the intensity of the band charge transfer with solvent polarity and a decrease in the intensity of the band of the locally excited state of anthracene. The fluorescence studies was al...
Apr 30, 2021Open Access
The aim of this work is to study the influence of the nature and position of substitution at allyl benzene on the regioselectivity of the hydrosilylation reaction. We studied hydrosilylation of the various allyl derivatives with cyclic siloxane, D 4H, and linears hydrosilylating agents, 1,1,3,3-tetramethyldisiloxane and MD HM, in the presence of platinum-based catalysts (Karstedt catalyst, platinum black). We also show the effects of the a...
Sep 18, 2019Open Access
The research was aimed at the antibacterial studies and cytotoxicity of aqueous trona extract of Sclerocarya birrea (marula) stem bark. Extraction of the stem bark was carried out using decoction method from the dried stem bark of marula. The extract was subjected to phytochemical screening, antibacterial and cytotoxicity test. The extract indicated the presence of tannin, saponins and alkaloids with the absenc ...
May 12, 2017Open Access
It has been shown by 1H
and 13C NMR spectroscopy that 2-mercaptobenzoyl-hydrazones of aliphatic
and aromatic aldehydes exist in solution as tautomeric mixtures of linear and
cyclic benzo-1,3,4-thiadiazepine forms. The linear hydrazone form is
represented by (E, ...
May 04, 2017Open Access
The thiazole derivative 3
was used for a series of heterocyclization reaction to produce pyran, pyridine
and thiazole derivatives. The cytotoxicity of the newly synthesized compounds
was studied against the six cancer cell lines namely NUGC, HR, DLD1, HA22T, HEPG2, MCF, HONE1 and
normal fibroblast cells (WI38). The results showed that most of the synthesized
compounds were of high potency. Amo ...
Jul 26, 2016Open Access
The present study focused on synthesizing a series of novel derivatives
of 4-aryl-1-[2-(3-benzyl-4-oxo(3H)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-2-ylsulphanyl)
acetyl] thiosemicarbazide 5a-d and evaluating their antitumor activity. The
structure of the synthesized compounds has been ...
May 23, 2016Open Access
The structure of the condensation products of thiobenzohydrazide,
2-sulfanylacetohydrazide, 3-sulfanylpropiohydrazide, and
2-sulfanylbenzohydrazide with a series of aldoses (L-arabinose, D-ribose,
L-rhamnose, D-galactose, D-glucose, and D-mannose) was studied by 1H-
and 13C-NMR spectro ...
May 04, 2016Open Access
The structure of the condensation products of
2-hydroxybenzohydrazide, 2-aminobenzohydrazide, and N-methyl-N-(2-aminobenzo) hydrazide with a series of aldoses
(L-arabinose, D-ribose, L- rhamnose, D-galactose, D-glucose, and D-mannose) was
studied by 1H- and 13C-NMR spectroscopy. The condensation
products of aldoses with 2-hydroxybenzohydrazide and 2-aminobenzohydra- zide in
DMSO d6 solutions exist as
equilibrium mixtures of linear acylhydrazone and cyclic p...
Apr 23, 2015Open Access
Diazotization and coupling of acetoacetanilide derivative 1 with aromatic amines afforded the arylhydrazones 2a,b. Arylhydrazones 2a,b were treated with (DMF-DMA) to yield the pyridazine derivatives 3a,b in good yield. Pyridazinone was treated with hydrazine hydrate to yield 4a,b. Reaction of 2a with hydroxylamine hydrochloride afforded the oxime derivative 5. Similarly, the reaction of acetoacetanilide 1 with hydroxylamine hydrochloride gave 3-hydroxyimino-N-p-tolyl- butyramide 8 not the pyrazo...
Feb 02, 2015Open Access
The in vitro anthelmintic evaluation of the
crude extracts and solvent partitions on Pheretima posthuma and Ascarissuum (eggs and L2 stage) respectively showed significant results at the same
concentration (10, 20, 40 and 80 mg/ml). This study
provides a clear evidence for usage of Mucuna pruriens and Canarium schweinfurthii as an anthelmintic. The most
potent ovicidal partition of C. schweinfurthii (Engl) leaves and bark and leaves
...
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