Asymmetric Dearomatization of 1‑Aminonaphthalene Derivatives by Gold-Catalyzed Intramolecular Double C–C Bond Formation

It has been established that a cationic gold­(I)/axially chiral biaryl bisphosphine complex catalyzes asymmetric dearomatization of 1-aminonaphthalene derivatives by the intramolecular double C–C bond formation. Two different dearomatization products were obtained depending on the substituents on the benzyl groups at the alkyne termini

Asymmetric Dearomatization of 1‑Aminonaphthalene Derivatives by Gold-Catalyzed Intramolecular Double C–C Bond Formation

It has been established that a cationic gold­(I)/axially chiral biaryl bisphosphine complex catalyzes asymmetric dearomatization of 1-aminonaphthalene derivatives by the intramolecular double C–C bond formation. Two different dearomatization products were obtained depending on the substituents on the benzyl groups at the alkyne termini

Asymmetric Dearomatization of 1‑Aminonaphthalene Derivatives by Gold-Catalyzed Intramolecular Double C–C Bond Formation

It has been established that a cationic gold­(I)/axially chiral biaryl bisphosphine complex catalyzes asymmetric dearomatization of 1-aminonaphthalene derivatives by the intramolecular double C–C bond formation. Two different dearomatization products were obtained depending on the substituents on the benzyl groups at the alkyne termini

Asymmetric Dearomatization of 1‑Aminonaphthalene Derivatives by Gold-Catalyzed Intramolecular Double C–C Bond Formation

It has been established that a cationic gold­(I)/axially chiral biaryl bisphosphine complex catalyzes asymmetric dearomatization of 1-aminonaphthalene derivatives by the intramolecular double C–C bond formation. Two different dearomatization products were obtained depending on the substituents on the benzyl groups at the alkyne termini