Enantioselective Synthesis of Bromodifluoromethyl-containing Oxazolines by Concerted Lewis/Bronsted Base Catalysis with Chiral Bisphosphine Oxide

We describe regio- and enantioselective bromocyclization of difluoroalkenes catalyzed by chiral bisphosphine oxides. Owing to the simultaneous activation of both the brominating reagent and amide substrate, the desired cyclization reaction proceeds smoothly even at low temperature to provide bromodifluoromethyl-containing oxazolines with a chiral quaternary center in a highly enantioselective fashion (up to 99% ee). This protocol features the use of commercially available brominating reagents and readily accessible chiral catalysts. The regioselectivity and enantioselectivity are influenced by the catalyst structure, the brominating reagent, and the reaction temperature. Under the optimal conditions, 5-exo cyclization proceeds preferentially compared with 6-endo cyclization, depending on the electronic properties of the alkene substrates. A gram-scale synthesis of chiral oxazoline was achieved with as little as 1 mol % of the catalyst.

Automated summary

We described regio- and enantioselective bromocyclization of difluoroalkenes catalyzed by chiral bisphosphine oxides. The reaction proceeds smoothly even at low temperature to provide bromodifluoromethyl-containing oxazolines with a chiral quaternary center in a highly enantioselective fashion. The protocol utilizes commercially available brominating reagents and readily accessible chiral catalysts, and the regioselectivity and enantioselectivity are influenced by the catalyst structure, the brominating reagent, and the reaction temperature. A gram-scale synthesis of chiral oxazoline was achieved with as little as 1 mol% of the catalyst.