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作 者:Weipeng Qi Xiaoqiang Xie Tengjiang Zhong Xingxian Zhang
机构地区:[1]College of Pharmaceutical Sciences, Zhejiang University of Technology
出 处:《Chinese Chemical Letters》2018年第1期194-196,共3页中国化学快报(英文版)
基 金:the National Natural Science Foundation of China (Nos. 21372203 and 21272076)for the financial support
摘 要:Direct aldol condensation of various aromatic, heteroaromatic, α,β-unsaturated aldehydes and aliphatic aldehydes with acyldiazomethane was realized using Mgl2 etherate (Mgl2.(Et2O)n) as a promoter in the presence of diisopropyl amine (DIPEA) in excellent yields in a short time under mild conditions with high chemoselectivity. Iodide counterion, and a non-coordinating less ploar reaction media (i.e., CH2C12) are among the critical factors for this unique reactivity.Direct aldol condensation of various aromatic, heteroaromatic, α,β-unsaturated aldehydes and aliphatic aldehydes with acyldiazomethane was realized using Mgl2 etherate (Mgl2.(Et2O)n) as a promoter in the presence of diisopropyl amine (DIPEA) in excellent yields in a short time under mild conditions with high chemoselectivity. Iodide counterion, and a non-coordinating less ploar reaction media (i.e., CH2C12) are among the critical factors for this unique reactivity.
关 键 词:ChemoselectiveAldehydeAcyldiazomethaneDirect aldol reactionMgl2 etherate
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