Axially Chiral Bridged Biaryls by Ni-Catalyzed Kinetic Asymmetric C–O Bond Cleavage DOI
Yijun Fang,

Jiameng Hu,

Tingting Sun

и другие.

ACS Catalysis, Год журнала: 2024, Номер 14(11), С. 8176 - 8183

Опубликована: Май 10, 2024

Axially chiral bridged biaryls represent an important subset of axially biaryl scaffolds in fields ranging from organic synthesis to biochemistry materials science. While numerous catalytic strategies have been elucidated for the construction axial chirality, enantioenriched form remains underdeveloped. Herein, we demonstrate approach synthesize diverse through nickel-catalyzed kinetic asymmetric cleavage unactivated aromatic C–O bond. The system features mild reaction conditions, high resolution efficiency, and versatile post-functionalizations. Mechanistic studies reveal impact nickel catalyst's chirality on stereochemical output this transformation.

Язык: Английский

Modular Assembly of Axially Chiral QUINAP Derivatives via Nickel-Catalyzed Enantioselective C–P Cross-Coupling DOI
Zhiping Yang,

Xiaodong Gu,

Li‐Biao Han

и другие.

ACS Catalysis, Год журнала: 2025, Номер unknown, С. 8268 - 8273

Опубликована: Май 2, 2025

Язык: Английский

Процитировано

0

Axially Chiral Bridged Biaryls by Ni-Catalyzed Kinetic Asymmetric C–O Bond Cleavage DOI
Yijun Fang,

Jiameng Hu,

Tingting Sun

и другие.

ACS Catalysis, Год журнала: 2024, Номер 14(11), С. 8176 - 8183

Опубликована: Май 10, 2024

Axially chiral bridged biaryls represent an important subset of axially biaryl scaffolds in fields ranging from organic synthesis to biochemistry materials science. While numerous catalytic strategies have been elucidated for the construction axial chirality, enantioenriched form remains underdeveloped. Herein, we demonstrate approach synthesize diverse through nickel-catalyzed kinetic asymmetric cleavage unactivated aromatic C–O bond. The system features mild reaction conditions, high resolution efficiency, and versatile post-functionalizations. Mechanistic studies reveal impact nickel catalyst's chirality on stereochemical output this transformation.

Язык: Английский

Процитировано

3