Different Performances of BF 3 , BCl 3 , and BBr 3 in Hypervalent Iodine-Catalyzed Halogenations.

Herein, hypervalent iodine-catalyzed halogenation of aryl-activated alkenes using BX 3 (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 3 resulted in different substitute sites from BBr 3 and BCl 3 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 3 was applied as the halogen source, while 1,2-aryl migration has "disappeared" when the halogen source was BBr 3 or BCl 3 . Possible catalytic cycles were proposed, and DFT calculations were conducted to demonstrate the differences among BX 3 (X = F, Cl, Br) in the hypervalent iodine-catalyzed halogenations.