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|Title:||Palladium-catalyzed allylic alkylation of enamides and allylic acetates||Authors:||Lim, Juan Mei||Keywords:||DRNTU::Science||Issue Date:||2012||Abstract:||Functionalization of enamides via allylic alkylation was achieved under the catalysis of palladium. The 5-membered N-(1H-inden-3-yl)acetamides afforded the corresponding allylic alkylation products 3 in high yields. On the other hand, the 6-membered N-(3,4- dihydronaphthalen-1-yl)acetamides besides giving 3 in moderate yields, also provided another product 3’, wherein the enamide functional group had been hydrolyzed to a ketone group.||URI:||http://hdl.handle.net/10356/47993||Fulltext Permission:||restricted||Fulltext Availability:||With Fulltext|
|Appears in Collections:||SPMS Theses|
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