Entity

Time filter

Source Type

Bandar Abbas, Iran

N-p-Methoxyphenyl, N-p-ethoxyphenyl, N-4-methoxynaphth-1-yl, and N-p-methoxybenzyl 2-azetidinones readily undergo oxidative N-dearylation to afford NH-2-azetidinones using a silver(II)-persulfate complex. The ease of preparation and stability of the reagents, neutrality of the reaction medium, fast conversions, good-to-excellent yields of products, and the mildness of the reaction conditions are some advantages of this method. © 2013 Elsevier Ltd. All rights reserved. Source


Homaei A.,Hormozgan University
Journal of Molecular Catalysis B: Enzymatic | Year: 2015

Alkaline phosphatase was purified from Fenneropenaeus merguiensis from Persian Gulf to homogeneity level by using (NH4)2SO4 precipitation, DEAE-cellulose and DEAE-Sephadex anion-exchange chromatography and gel filtration chromatography. The molecular weight of the enzyme was 70 kDa, measured by SDS-PAGE. The alkaline phosphatase showed the strongest affinity with p-NPP as the substrate, and the highest catalytic efficiency for hydrolysis of the substrate at pH 11 and 50 °C. Activation energy (Ea) for catalysis of alkaline phosphatase was 8.3 kcal mol-1 K-1, while temperature quotient (Q10) was 3.25. It exhibited Michaelis-Menten kinetics with kcat of 95 s-1 and Km of 0.3 μM, respectively. Thermodynamic parameters for soluble p-NPP hydrolysis were as follows: ΔH# = 7.7 kcal mol-1 K-1, ΔG# = 14.7 kcal mol-1 K-1, ΔS# = -23.5 cal mol-1 K-1, ΔGE-S#=-0.7 kcal mol-1K-1 and ΔGE-T#=-3.4 kcal mol-1 K-1. Thermodynamic parameters (ΔH∗, ΔG∗, ΔS∗) for irreversible inactivation of alkaline phosphatase at different temperatures (35-50 °C) were also determined. © 2015 Elsevier B.V. All rights reserved. Source


Zarei M.,Hormozgan University
Bulletin of the Chemical Society of Japan | Year: 2012

An efficient one-pot synthesis of β-lactams by the reaction of imines with acetic acid derivatives in the presence of DMF and benzoyl chloride adduct, a cheap reagent, has been described. Optimization of solvents, temperature, and molar ratio of reagent was also performed. Several types of β-lactams including monocyclic, spirocyclic, N-alkyl, 3-butadienyl, and 3-electron-withdrawing group have been synthesized by this method in good to excellent yields. All steps of the reaction proceed at room temperature. © 2012 The Chemical Society of Japan. Source


Homaei A.,Hormozgan University
International Journal of Biological Macromolecules | Year: 2015

Immobilization of papain was carried out by covalent attachment on Sepharose 6B activated by using cyanogen bromide. Immobilization process brought about significant enhancement of storage and thermal stability, stability at extreme pHs, and resistance against the inhibitory effects of various bivalent metal ions with respect to papain. The optimum temperature of papain increased by 20°C (from 60 to 80°C) and its optimum pH was shifted from 6.5 to 8.0 upon immobilization. The activation energy of the enzymatic reaction for immobilized papain showed a significant increase as compared with its free form (1.87kcalmol-1K-1 for free and 4.69kcalmol-1K-1 for immobilized enzyme). The kinetic parameters, Km and kcat, were estimated to be 0.62μM and 162×10-4s-1 for free and 0.79μM and 102×10-4s-1 for immobilized papain, respectively. © 2015 Elsevier B.V. Source


Zarei M.,Hormozgan University
Monatshefte fur Chemie | Year: 2013

The application and versatility of 2-fluoro-1-methylpyridinium p-toluenesulfonate as acid activator in the synthesis of several β-lactams under mild reaction conditions by use of ketene-imine cycloaddition reactions has been investigated. The effects of solvents, molar ratio of reagents, and temperature were considered. The method was also used for preparation of β-lactams substituted in position 3 by electron-withdrawing groups. The products are obtained in good to excellent yields. © 2013 Springer-Verlag Wien. Source

Discover hidden collaborations