Biochemistry
Mohammad Ali Nasseri; Soheila Behravesh; Ali Allahresani
Volume 5, Issue 4, pp. 364-493, Serial No. 17 , October 2017, , Pages 364-371
Abstract
In this study, the essential oil content in the aerial parts of Cleome heratensis which is growing in the east of Iran was investigated. The aerial parts of the plant were collected from the late August to October 2014, for a total of four harvests (S1-S4). Essential oils were isolated by hydro-distillation. ...
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In this study, the essential oil content in the aerial parts of Cleome heratensis which is growing in the east of Iran was investigated. The aerial parts of the plant were collected from the late August to October 2014, for a total of four harvests (S1-S4). Essential oils were isolated by hydro-distillation. The oils were analyzed by GC-FID and 30 constituents, representing 84.93-92.9 % of the total compositions of the oil were identified. The major components of the essential oil in the four harvests were hexanal (7.57%-33.96%), α-phellandrene (6.08% -13.17%), α-farnesen (7.54%-10.9%), methyl eugenol (6.74%-8.31%), eugenol (3.94%-7.4%), verbenone (3.98%-6.24%), myrcene (1.54%-5.75%), hexadecane (2.34%-4.82%), linalool (1.59% - 3.53%) and α-humulene (1.01%-1.93%). The findings indicated That the main component groups of oil are monoterpenoids (11.83–19.29%), oxygenated monoterpens (10.34–16.96%), sesquiterpenoids (10.67–20%) and oxygenated sesquiterpenes (0–4.34%) which are obviously increased during the growing stages. Monoterpenoids were higher during the late flowering stage (S3), but oxygenated monoterpens were observed to be slightly lower in this stage. Monoterpens are slightly higher during development stages.
Nanochemistry
Mohammad Ali Nasseri; Batol Zakerinasab; Sayyde Kamayestani
Volume 4, Issue 3, pp. 236-358, Serial No. 12 , July 2016, , Pages 283-294
Abstract
Mn(II) salen complex immobilized on nano silicagel was prepared by incorporating Mn(II) salen complex into a nanosilica matrix and characterized by TGA, XRD, atomic absorption spectroscopy and was successfully applied as catalyst for the oxidation of alcohols. Oxidation of a series of alcohols in acetonitrile ...
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Mn(II) salen complex immobilized on nano silicagel was prepared by incorporating Mn(II) salen complex into a nanosilica matrix and characterized by TGA, XRD, atomic absorption spectroscopy and was successfully applied as catalyst for the oxidation of alcohols. Oxidation of a series of alcohols in acetonitrile over immobilized Mn(II) salen complex using tetrabutylammonium peroxymonosulfate (TBAO) as oxidant were resulted to the corresponding carbonyl compounds selectively in moderate to high yields. It is noteworthy that the aldehydes do not undergo further oxdation to carboxylic acids. The yields of aromatic alcohols are higher than those of alcohols with aliphatic groups. The catalyst has been reused several times, without observable loss of its activity and selectivity.
Organic chemistry
Batol Zakerinasab; Mohammad Ali Nasseri; Fateme Kamali
Volume 3, Issue 4, pp. 283-387, Serial No. 9 , October 2015, , Pages 335-347
Abstract
Quinolines, an important class of potentially bioactive compounds, have been synthesized by treatment of O-aminoarylketones and carbonyl compounds utilizing niobium (V) chloride / polyethylenglycole(NbCl5.PEG) and niobium(V)chloride (NbCl5) as available and inexpensive catalysts. The quinoline derivatives ...
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Quinolines, an important class of potentially bioactive compounds, have been synthesized by treatment of O-aminoarylketones and carbonyl compounds utilizing niobium (V) chloride / polyethylenglycole(NbCl5.PEG) and niobium(V)chloride (NbCl5) as available and inexpensive catalysts. The quinoline derivatives were prepared in glycerol, an excellent solvent in terms of environmental impact, with high yields (76-98%) and short reaction times (15- 90 min). Not only diketones but also ketones afforded the desired products in good to excellent yields. The reaction time of 2-amino-5-chlorobenzophenone and dicarbonyl compounds was longer than those of 2-aminobenzophenone. The reaction of cyclic diketones took place faster than open chain analogues. These reactions also proceeded with acetophenone derivatives. In these cases the reaction times are longer.
Biochemistry
Mohammad Ali Nasseri; Zahra Kakouee; Ali Allahresani
Volume 3, Issue 3, pp. 180-282,Serial No. 8 , July 2015, , Pages 180-186
Abstract
Artemisia deserti Krasch (A. deserti), Artemisia aucheri (A. aucheri) and Artemisia sieberi Besser (A. sieberi) are three members of Asteraceae (compositae) family, which grow widely in the even and high areas of Birjand, Iran. This study has attempted to compare the total antioxidant capacity of methanol ...
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Artemisia deserti Krasch (A. deserti), Artemisia aucheri (A. aucheri) and Artemisia sieberi Besser (A. sieberi) are three members of Asteraceae (compositae) family, which grow widely in the even and high areas of Birjand, Iran. This study has attempted to compare the total antioxidant capacity of methanol extracts of these three plants using DPPH (1,1-Diphenyl-2-Picrylhydrazyl) radical scavenging assay in which spectrophotometry method was used at 517 nm. The results showed that the aerial parts (AP) of A. sieberi has the highest total antioxidant capacity (IC50=11.054 mg/mL). The lowest amount of antioxidant capacity was found in the root (R) of A. aucheri (IC50= 91.408 mg/mL).
Organic chemistry
Mohammad Ali Nasseri; Ali Allahresani; Batol Zakeri Nasab
Volume 3, Issue 2, pp. 72-147, Serial No. 7 , April 2015, , Pages 78-85
Abstract
Microwave assisted green synthesis of α, ά- bis (substituted- benzylidene) alkanones by the crossed- aldol condensation reaction of substituted aryl aldehydes with ketones in the presence of catalytic amount of NbCl5 in good to excellent yields. This reaction is carried out under solvent-free ...
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Microwave assisted green synthesis of α, ά- bis (substituted- benzylidene) alkanones by the crossed- aldol condensation reaction of substituted aryl aldehydes with ketones in the presence of catalytic amount of NbCl5 in good to excellent yields. This reaction is carried out under solvent-free conditions. The results showed that aldehydes bearing electron–donating substituent's on phenyl-ring favored the formation of product in good to excellent yields with reaction times ranging between 3 and 7 min. In addition, furfural, cinamaldehyde, thiophene-2-carbaldehyde and 5-methylthiophene-2-carbaldehyde were investigated in aldol reaction, and the results showed excellent yields. Also, the reactions were carried out at room & thermal (80 0C) conditions. The results showed that the yields are in accordance with the microwave irradiations, But the time is 1.5-5 h at room temperature and 15-45 min in thermal conditions.