Rhodium‐Catalyzed Direct ortho‐Arylation of Anilines DOI
Clément Jacob, Julien Annibaletto,

Ju Peng

et al.

Angewandte Chemie, Journal Year: 2024, Volume and Issue: 136(30)

Published: April 29, 2024

Abstract An efficient and broadly applicable rhodium‐catalyzed direct ortho ‐arylation of anilines with aryl iodides relying on readily available aminophosphines as traceless directing groups is reported. Its scope functional group compatibility were both found to be quite broad a large variety (hetero)aryl iodides, including complex ones, could utilized. The ‐arylated obtained in high average yields, without any competing diarylation full regioselectivity, which constitutes major step forward compared other processes. reaction moreover not limited an bromide triflate successfully used, extended diarylation. Mechanistic studies revealed the key unique role aminophosphine, acting only substrate but also ligand for rhodium catalyst.

Language: Английский

Rhodium‐Catalyzed Direct ortho‐Arylation of Anilines DOI
Clément Jacob, Julien Annibaletto,

Ju Peng

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(30)

Published: April 29, 2024

Abstract An efficient and broadly applicable rhodium‐catalyzed direct ortho ‐arylation of anilines with aryl iodides relying on readily available aminophosphines as traceless directing groups is reported. Its scope functional group compatibility were both found to be quite broad a large variety (hetero)aryl iodides, including complex ones, could utilized. The ‐arylated obtained in high average yields, without any competing diarylation full regioselectivity, which constitutes major step forward compared other processes. reaction moreover not limited an bromide triflate successfully used, extended diarylation. Mechanistic studies revealed the key unique role aminophosphine, acting only substrate but also ligand for rhodium catalyst.

Language: Английский

Citations

3

Rhodium‐Catalyzed Direct ortho‐Arylation of Anilines DOI
Clément Jacob, Julien Annibaletto,

Ju Peng

et al.

Angewandte Chemie, Journal Year: 2024, Volume and Issue: 136(30)

Published: April 29, 2024

Abstract An efficient and broadly applicable rhodium‐catalyzed direct ortho ‐arylation of anilines with aryl iodides relying on readily available aminophosphines as traceless directing groups is reported. Its scope functional group compatibility were both found to be quite broad a large variety (hetero)aryl iodides, including complex ones, could utilized. The ‐arylated obtained in high average yields, without any competing diarylation full regioselectivity, which constitutes major step forward compared other processes. reaction moreover not limited an bromide triflate successfully used, extended diarylation. Mechanistic studies revealed the key unique role aminophosphine, acting only substrate but also ligand for rhodium catalyst.

Language: Английский

Citations

0