Magnesium bistrifluoromethanesulfonimide as an efficient catalyst for the hydroalkylation of aromatic olefins with 1,3-diketones under solvent-free conditions
摘要:
An efficient magnesium bistrifluoromethanesulfonimide [Mg(NTf(2))(2)] catalyzed hydroalkylation of aromatic olefins with 1,3-diketones under solvent-free conditions has been developed. The reactions proceed smoothly to give the desired products in good yields in short reaction times. (C) 2011 Hong She Wang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
The vinyl arenes undergo smooth hydroalkylation with 1,3-diketones in the presence of 10 mol% of iodine to afford phenethyl diketones and ketoesters in good yields in short reaction times. The use of inexpensive and readily available molecular iodine makes this method quite simple, more convenient and practical. (C) 2010 Elsevier Ltd. All rights reserved.
Magnesium bistrifluoromethanesulfonimide as an efficient catalyst for the hydroalkylation of aromatic olefins with 1,3-diketones under solvent-free conditions
作者:Hong She Wang、Wei Xing Zhao
DOI:10.1016/j.cclet.2011.01.036
日期:2011.8
An efficient magnesium bistrifluoromethanesulfonimide [Mg(NTf(2))(2)] catalyzed hydroalkylation of aromatic olefins with 1,3-diketones under solvent-free conditions has been developed. The reactions proceed smoothly to give the desired products in good yields in short reaction times. (C) 2011 Hong She Wang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.