شماره ركورد كنفرانس :
3776
عنوان مقاله :
Direct synthesis of Symmitrical disulfid from aril halydes with a Novel sulfur source in the presence of copper nanoparticles
پديدآورندگان :
Akbari Zahra Ilam University , Soliman-beigi Mohammad SoleimanBeigi@yahoo.com Ilam University
تعداد صفحه :
1
كليدواژه :
,
سال انتشار :
1395
عنوان كنفرانس :
بيست چهارمين سمينار شيمي آلي ايران
زبان مدرك :
انگليسي
چكيده فارسي :
Organic sulfides are important compounds which widely exist in many biologically and pharmaceutically active molecules. Especially sulfides moieties have been used in the treatment diseases such as Parkinson,s, Alzheimer,s, immune and inflammatory, diabetes, HIV.The formation of carbon-sulfur bond has been widely examined and generally from nano particles catalyzed for coupling bond C-S have been used for the formation this bond., For example disulfide bondes have been employed in stabilization of peptides in proteins, DNA cleaving and design of drug delivery systems [1]. Copper nanoparticles catalyst was easily isolated from the reaction mixture by simple filtration and reused with loss in activity Using nontoxic and nano catalyst, simplified operational process, short reaction times purification of the products without using chromatographic separation, and environmentally, and excellent yield [2]. As part of our current studies on the synthesis of organosulfurs compounds, we report the results of our studies involving the reaction between aryl halides with 1,3,4-Thiadiazol- 2,5dithiol in the present of copper nanoparticles as a catalyst, KOH as a base at 100 oC in Wet Appropriate solvent . High yields were obtained and cooper nanoparticles catalyst was easily isolated from the reaction mixture by simple filtration and reused with loss in activity.
كشور :
ايران
لينک به اين مدرک :
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