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• W4366608227 startingPage "110132" @default.
• W4366608227 abstract "Bromination of ten known fluorinated quinolin-2(1H)-ones by the KBrO3/HBr system is investigated. If there is no F atom in the position 6 of substrate, the Br atom is introduced into position 3 or 6 to form monobromo derivative, the second Br atom is introduced into the same positions leading to 3,6-dibromo product. If a F atom is in position 6, the 3-bromo product is initially obtained, which gives a 3,5-dibromo or 3,8-dibromo derivatives upon further bromination depending on the F atoms positions. In this case, when both positions 5 and 8 of 3-bromoquinolin-2(1H)-one are unsubstituted, the second Br atom is introduced into position 8. If there are more than two F atoms in the benzene moiety, the sole 3-bromo product is obtained. Relative (ΔE) energies of the considered σ−complexes estimated by DFT calculations for the reactions in question are consistent with the experimentally observed regioselectivity." @default.
• W4366608227 created "2023-04-23" @default.
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• W4366608227 date "2023-05-01" @default.
• W4366608227 modified "2023-09-24" @default.
• W4366608227 title "Bromination of quinolin-2(1H)-ones fluorinated on the benzene moiety" @default.
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• W4366608227 doi "https://doi.org/10.1016/j.jfluchem.2023.110132" @default.
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