Different Performances of BF, BCl, and BBr in Hypervalent Iodine-Catalyzed Halogenations.

Herein, hypervalent iodine-catalyzed halogenation of aryl-activated alkenes using BX (X = Cl, Br) as the halogen source and activating reagents was reported. Various halogenated 1,3-oxazine/2-oxazoline derivatives were obtained in good-to-high yields. Using BF resulted in different substitute sites from BBr and BCl of the products, indicating different reactive intermediates and reaction pathways. The reaction underwent a "ligand coupling/oxidative addition/intermolecular nucleophilic attack/1,2-aryl migration/reductive elimination/intramolecular nucleophilic attack" cascade when BF was applied as the halogen source, while 1,2-aryl migration has "disappeared" when the halogen source was BBr or BCl. Possible catalytic cycles were proposed, and DFT calculations were conducted to demonstrate the differences among BX (X = F, Cl, Br) in the hypervalent iodine-catalyzed halogenations.