
Tetrahedron Chem, Год журнала: 2025, Номер 14, С. 100133 - 100133
Опубликована: Май 10, 2025
Язык: Английский
Tetrahedron Chem, Год журнала: 2025, Номер 14, С. 100133 - 100133
Опубликована: Май 10, 2025
Язык: Английский
Organic & Biomolecular Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
2,2-Disubstituted indolin-3-ones, which are essential components in many manufactured chemicals, dyes, and naturally occurring bioactive alkaloids, have emerged as exciting synthetic targets. Much attention has been paid to accessing these units, particularly an asymmetric fashion, during the last decade. In this review article, we discuss current state of available methods with existing mechanistic pathways for chiral indolin-3-one derivatives under various catalytic systems. This overall presentation protocols access 2,2-disubstituted or fused indolin-3-ones aza-quaternary centre is categorized based on reaction modes 2-substituted-3H-indole-3-one other similar protocols.
Язык: Английский
Процитировано
0Tetrahedron Chem, Год журнала: 2025, Номер 14, С. 100133 - 100133
Опубликована: Май 10, 2025
Язык: Английский
Процитировано
0