7 research outputs found
Enantioselective Bromocyclization of Olefins Catalyzed by Chiral Phosphoric Acid
A chiral phosphoric acid catalyzed enantioselective bromocyclization of olefins is described. Various <i>cis</i>-, <i>trans</i>-, or trisubstituted γ-hydroxy-alkenes and γ-amino-alkenes can cyclize under the reaction conditions to give optically active 2-substituted tetrahydrofurans and tetrahydropyrroles in up to 91% ee
Enantioselective Bromocyclization of Olefins Catalyzed by Chiral Phosphoric Acid
A chiral phosphoric acid catalyzed enantioselective bromocyclization of olefins is described. Various <i>cis</i>-, <i>trans</i>-, or trisubstituted γ-hydroxy-alkenes and γ-amino-alkenes can cyclize under the reaction conditions to give optically active 2-substituted tetrahydrofurans and tetrahydropyrroles in up to 91% ee
Enantioselective Bromocyclization of Olefins Catalyzed by Chiral Phosphoric Acid
A chiral phosphoric acid catalyzed enantioselective bromocyclization of olefins is described. Various <i>cis</i>-, <i>trans</i>-, or trisubstituted γ-hydroxy-alkenes and γ-amino-alkenes can cyclize under the reaction conditions to give optically active 2-substituted tetrahydrofurans and tetrahydropyrroles in up to 91% ee