Cupric chloride promoted regioselective C-allylation of enaminones
摘要:
Regioselective allylation of enaminones using CuCl2 as the catalyst to give C-allylated products is reported for the first time. The C-allylated products undergo hydrolysis followed by a rearrangement yielding beta-keto allyl enamides in excellent yields. (C) 2008 Elsevier Ltd. All rights reserved.
Regioselective allylation of enaminones using CuCl2 as the catalyst to give C-allylated products is reported for the first time. The C-allylated products undergo hydrolysis followed by a rearrangement yielding beta-keto allyl enamides in excellent yields. (C) 2008 Elsevier Ltd. All rights reserved.