Mild and efficient barbier allylation reaction mediated by magnesium powder under solvent-free conditions

Abstract

A novel and highly efficient synthesis of homoallylic alcohols is achieved by the allylation of carbonyl compounds using magnesium powder as mediator under solvent-free conditions. A series of aldehydes and ketones are converted to the corresponding homoallylic alcohols, the yields of the reaction is considerably high (85–98%). The procedure is environment benign, operationally simple and easy to scale up at room temperature.