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.