Morita–Baylis–Hillman Reaction of α,β-Unsaturated Ketones with Allylic Acetates by the Combination of Transition-Metal Catalysis and Organomediation
作者:Ya-Qiong Li、Hai-Jun Wang、Zhi-Zhen Huang
DOI:10.1021/acs.joc.6b00684
日期:2016.6.3
An intermolecular Morita–Baylis–Hillman (MBH) reaction of α,β-unsaturatedketones with allylic acetates under the catalysis of 10 mol % of tetrakis(triphenylphosphine)palladium(0) and mediation of tributylphosphine has been developed in the presence of acetic acid, affording the desired α-coupling products. The MBH reaction has the advantages of good tolerance to many functional groups, excellent regioselectivity
A range of ketone-stabilized phosphoniumylides were allylated with high regioselectivity by primary allylic amines in the presence of 5 mol % Pd(PPh3)4 and 10 mol % B(OH)3, and subsequent one-pot Wittig olefination gave structurally diverse α,β-unsaturated ketones in good to excellent overall yields with excellent E selectivity. The one-pot allylation/olefination reaction was extended to ester- and