Woerly, Eric M.; Banik, Steven M.; Jacobsen, Eric N. published the artcile< Enantioselective, Catalytic Fluorolactonization Reactions with a Nucleophilic Fluoride Source>, Related Products of 6942-39-8, the main research area is fluoroisochromanone enantioselective synthesis regioselectivity; alkenyl benzoate preparation fluorolactonization; bromobenzoate alkenyl boronic acid pinacol ester.
The enantioselective synthesis of 4-fluoroisochromanones via chiral aryl iodide-catalyzed fluorolactonization is reported. This methodol. uses HF-pyridine as a nucleophilic fluoride source with a peracid stoichiometric oxidant and provides access to lactones containing fluorine-bearing stereogenic centers in high enantio- and diastereoselectivity. The regioselectivity observed in these lactonization reactions is complementary to that obtained with established asym. electrophilic fluorination protocols.
Journal of the American Chemical Society published new progress about Enantioselective synthesis. 6942-39-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H6BrFO2, Related Products of 6942-39-8.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary