REMOTE SUBSTITUENT EFFECTS IN THE BAEYER-VILLIGER OXIDATION. I. THROUGH-BOND γ SUBSTITUENT EFFECT ON THE REGIOSELECTIVITY

Article abstract of DOI:10.1016/0040-4039(80)80132-8

Regioselectivity of the Baeyer-Villiger oxidation of 8-oxabicyclo<3.2.1>octan-3-one derivatives is markedly affected by the electronic nature of substituents at position γ to the carbonyl function.