Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 355 - 393
Опубликована: Янв. 1, 2024
Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 355 - 393
Опубликована: Янв. 1, 2024
Organic Letters, Год журнала: 2025, Номер unknown
Опубликована: Фев. 2, 2025
Palladium-catalyzed asymmetric intermolecular trans-acetoxypalladation/desymmetric cyclization/acyl transfer cascades of alkyne-tethered malononitriles with carboxylic acids have been demonstrated. Such a sequence enables the formation multifunctionalized nitriles bearing α-all-carbon quaternary stereocenters high degree enantiocontrol broad substrate scope. Moreover, synthetic elaborations present these molecules as promising chiral building blocks. Mechanistic studies illustrate that cascade process proceeds via key imine intermediate, and desymmetric cyclization is enantio-determining step.
Язык: Английский
Процитировано
0The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 11, 2025
A new approach to multifunctionalized pyrroles has been explored by the tandem cyclization of α-oxoketene-N,S-acetals with β-ketodinitriles using Cu(MeCN)4BF4 and Ag2CO3 in toluene under reflux conditions. The reaction involves C–C/C–N bond creation, is assumed proceed via enamine formation, intramolecular cyclization, rearrangement. potential methodology also demonstrated for a gram-scale as well some useful organic transformations. offers practical pathway achieve polysubstituted broad substrate scope good functional group tolerance.
Язык: Английский
Процитировано
0Journal of Molecular Structure, Год журнала: 2025, Номер 1338, С. 142312 - 142312
Опубликована: Апрель 14, 2025
Язык: Английский
Процитировано
0Journal of Chemical Sciences, Год журнала: 2025, Номер 137(2)
Опубликована: Май 17, 2025
Язык: Английский
Процитировано
0Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 355 - 393
Опубликована: Янв. 1, 2024
Процитировано
0