Tetrahedron Letters, Год журнала: 2025, Номер 158, С. 155472 - 155472
Опубликована: Фев. 20, 2025
Язык: Английский
Tetrahedron Letters, Год журнала: 2025, Номер 158, С. 155472 - 155472
Опубликована: Фев. 20, 2025
Язык: Английский
Organic Letters, Год журнала: 2025, Номер unknown
Опубликована: Март 3, 2025
A novel and efficient method for the synthesis of multisubstituted arylnitriles via Tf2O-mediated [3 + 2 1] benzannulation enaminones acylacetonitriles has been developed. This reaction proceeds under mild conditions with excellent functional group compatibility. Mechanistic studies have revealed that cyclization involves two consecutive nucleophilic additions, followed by a cascade Knoevenagel condensation aromatization. Additionally, trifluoromethanesulfonate 6 identified as crucial intermediate in this process.
Язык: Английский
Процитировано
1Tetrahedron Letters, Год журнала: 2025, Номер 158, С. 155472 - 155472
Опубликована: Фев. 20, 2025
Язык: Английский
Процитировано
0