M. S. Shiri Shahraki

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In the present work, for the first time, investigation of the initial fast step of reaction between 1,1,1-trichloro-3-methyl-3-phospholene (TCMP) and methanol was studied under a dry inert atmosphere by a newly constructed CSF apparatus by means of a further development in the configuration of the previous stopped-flow spectrophotometer (SFS). Hence, it was(More)
Dynamic (1)H NMR measurements were performed within the synthesized particular phosphorus ylide involving 4-formylphenyl phenylcarbamate. Four rotational process and thereby parameters were targeted for rotation around the CC, C-C, HCNC and OCNC bonds. The Gibbs free activation energy in CDCl3, ΔG(≠)exp, was found to be 64 ± 2, 50 ± 2, 41 ± 2 and 63 ± 2,(More)
Inhibition efficiencies of three amino acids [tryptophan (B), tyrosine (c), and serine (A)] have been studied as green corrosion inhibitors on corrosion of carbon steel using density functional theory (DFT) method in gas and aqueous phases. Quantum chemical parameters such as EHOMO (highest occupied molecular orbital energy), ELUMO (lowest unoccupied(More)
AIM AND OBJECTIVE Tetrahydrobenzo[b]pyran derivatives are considered as a special class in drug research because of their various biological and pharmacological benefiting usages. In the current work, we developed new synthetic methods for the preperation of tetrahydrobenzo[b]pyran derivatives using arylaldehydes 1, malononitrile 2 and dimedonein 3 in the(More)
The kinetics of the reaction between triphenylphosphine (TPP) and dimethyl acetylenedicarboxylate (DMAD) in the presence of Meldrum's acid (MA) for the generation of the 1,4-diionic organophosphorus compound has been investigated using the stopped-flow and UV-VIS spectrophotometry techniques. The first step of the reaction between TPP and DMAD for the(More)
The hindered internal rotations around the partial carbon-carbon double bond, nitrogen-carbon and carbon-carbon single bonds within the 2-(2-chloro-phenothiazine-l-yl)-3-(triphenylphosphoranylidene) butandioate has been experimentally studied by the dynamic H NMR spectroscopic in variable temperatures. The activation (∆H, ∆S, ∆G) and kinetic (kc, Ea)(More)
An efficient synthesis of 1,3-oxathiolan-2-yliden derivatives is described via a simple reactions between CHacids, CS2 and oxiranes in the presence of triethylamine at 70° C in water as the solvent. The mild reaction conditions and high yields of the products exhibit the good synthetic advantage of this method.