|
|
Go
Feb 27, 2025Open Access
Photochemical bromination of toluene up to 300 mmol per run in aqueous biphasic system formed benzyl bromide of sufficient purity to be used directly for benzylations without any purification. 1-Methylnaphthalene and acetophenone react similarly. An approach to (R) and (S) 1-O-triphenylmethyl-glycerol is presented based on L- and D-xylose.
Jan 27, 2025Open Access
A series of pyrazole and pyridazine derivatives and their Schiff bases were synthesized and tested for their antibacterial and antioxidant activities. The prepared compounds were analyzed using infrared, 1H NMR, and mass spec-trometry. Studies of the antibacterial and antioxidant compounds showed promising antibacterial and antioxidant activities.
Jul 15, 2024Open Access
We report here a complete study of coordination of the 5-aminomethyl- [13]aneN 4 with chromophoric groups (anthracene, pyrene and naphtalene) by four metals: Zn(II), Cu(II), Ni(II) and Cr(III). We aim to study the effect of the C-functionalization of the macrocycle on the stability of the metal complexes and the size of the metal impact on the quenching of fluorescence of the chromophoric groups. The results obtained by spectrometry, EPR and X-ray of the metal complexes confirm that th...
Oct 30, 2023Open Access
We report here a complete study of coordination of the 5-aminomethyl-[13] aneN 4 ligand by three metals: Cu(II), Ni(II) and Cr(III) in order to determine the effect of the C-functionalization of the macrocycle on the stability of the metal complexes even if we change the size of the metal used. The results obtained by spectrometry, EPR and X-ray of the metal complexes showed that the copper is pentacoordinate in square-based pyramidal environment, but the chromium and nickel complexes ...
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 ...
Go
|
|
|
