Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 211 - 257
Опубликована: Янв. 1, 2024
Язык: Английский
Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 211 - 257
Опубликована: Янв. 1, 2024
Язык: Английский
Chemistry - A European Journal, Год журнала: 2024, Номер 30(57)
Опубликована: Авг. 1, 2024
In this work, we used photoinert anhydrous cerium(III) chloride, to form a transient charge-transfer (CT) complex with NXS (N-bromosuccinimide or NBS and N-iodosuccinimide NIS) in acetonitrile. These CT complexes acted as semi-heterogeneous photocatalyst. allowed the Ce(III) ions absorb light, turning them into strong electron donors that transferred electrons NXS. This created halide radicals from radical anions, helping turn N-propargylamides oxazole aldehydes. Experiments DMPO spin-trapping showed radical-based mechanism followed single transfer (SET) pathway. Notably, CeCl
Язык: Английский
Процитировано
1Asian Journal of Organic Chemistry, Год журнала: 2024, Номер 13(6)
Опубликована: Апрель 3, 2024
Abstract An efficient one‐pot synthesis of 1 H ‐pyrazoles has been realized via cascade cyclocondensation β‐nitroalkenes as C2 synthon with α‐diazoesters C1N2 unit. The reaction proceeds concomitant formation two new (C−N & C−C) bonds in one stretch leading to ethyl‐5‐nitro‐4‐phenyl‐4,5‐dihydro‐3 ‐pyrazole‐3‐carboxylate intermediate, which undergoes base mediated denitration enabling the NH−pyrazoles. This protocol not only features easy operation, catalyst−free conditions, good high yields, wide scope and late‐stage functionalization, but also opens up a avenue for synthetically demanding structurally non‐traditional pyrazoles. A combination experimental DFT studies provide evidence proposed mechanism.
Язык: Английский
Процитировано
0Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 211 - 257
Опубликована: Янв. 1, 2024
Язык: Английский
Процитировано
0