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   Asymmetric epoxidation of chalcones promoted by chiral schiff bases and amino alcohols  
   
نویسنده shen t. ,li j. ,cui f. ,zhou x. ,chen x. ,song q.
منبع journal of the chemical society of pakistan - 2013 - دوره : 35 - شماره : 5 - صفحه:1354 -1358
چکیده    A series of chiral ligands were conveniently prepared from l-phenylalanine and characterized. their application to the asymmetric epoxidation of chalcone was studied. the results demonstrated that 3a were efficient catalysts for enantioselective epoxidation of chalcone in moderate yield (up to 58.6%) and high enantioselectivities (up to 90% e.e.).
کلیدواژه Asymmetric epoxidation; Chiral ligands; Enantioselective.; L-phenylalanine
آدرس state key laboratory breeding base of green chemistry - synthesis technology,zhejiang,university of technology, China, state key laboratory breeding base of green chemistry - synthesis technology,zhejiang,university of technology, China, state key laboratory breeding base of green chemistry - synthesis technology,zhejiang,university of technology, China, state key laboratory breeding base of green chemistry - synthesis technology,zhejiang,university of technology, China, state key laboratory breeding base of green chemistry - synthesis technology,zhejiang,university of technology, China, state key laboratory breeding base of green chemistry - synthesis technology,zhejiang,university of technology, China
 
     
   
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