New Journal of Chemistry, Год журнала: 2023, Номер 48(2), С. 733 - 737
Опубликована: Дек. 1, 2023
A metal-free strategy to 2-aryl-3-(2-aminoaryl)quinoxalines from 2-alkynylnitrobenzenes and 1,2-diaminobenzenes is developed.
Язык: Английский
New Journal of Chemistry, Год журнала: 2023, Номер 48(2), С. 733 - 737
Опубликована: Дек. 1, 2023
A metal-free strategy to 2-aryl-3-(2-aminoaryl)quinoxalines from 2-alkynylnitrobenzenes and 1,2-diaminobenzenes is developed.
Язык: Английский
Опубликована: Янв. 1, 2024
Язык: Английский
Процитировано
0Опубликована: Янв. 1, 2023
Herein we report the regioselective cyanation of isatogen (3-indolone N-oxide) and its derivatives. The high electrophilicity is a key feature for their various chemical transformations, describe new application to use boron catalyst regio- stereoselective at C2 position isatogen. combination B(C6F5)3 Me3SiCN optimal, C2-cyano adducts are exclusively obtained in up quantitative yield. In addition, isatogenol that includes tertiary hydroxyl group C3 also suitable this create consecutive tetra-substituted carbons with stereoselectivity.
Язык: Английский
Процитировано
0New Journal of Chemistry, Год журнала: 2023, Номер 48(2), С. 733 - 737
Опубликована: Дек. 1, 2023
A metal-free strategy to 2-aryl-3-(2-aminoaryl)quinoxalines from 2-alkynylnitrobenzenes and 1,2-diaminobenzenes is developed.
Язык: Английский
Процитировано
0