Mild Base Promoted Nucleophilic Substitution of Unactivated sp3‐Carbon Electrophiles with Alkenylboronic Acids

Abstract Diverse alkenylboronic acids react smoothly with various sp3‐carbon electrophiles such as unactivated alkyl triflates in the presence of mild bases such as K3PO4. The reaction protocol is very mild and thereby enables high functional group tolerance. This transition metal‐free condition is orthogonal towards the classic transition metal catalyzed Suzuki coupling. magnified image