Elsevier eBooks, Год журнала: 2024, Номер unknown, С. 151 - 219
Опубликована: Авг. 16, 2024
Язык: Английский
Elsevier eBooks, Год журнала: 2024, Номер unknown, С. 151 - 219
Опубликована: Авг. 16, 2024
Язык: Английский
Organic & Biomolecular Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
Recent advances in the photo-promoted C3–H alkylation reaction of quinoxalin-2(1 H )-ones with different agents.
Язык: Английский
Процитировано
0Organic & Biomolecular Chemistry, Год журнала: 2023, Номер 21(40), С. 8136 - 8140
Опубликована: Янв. 1, 2023
The widespread presence of bicyclo[1.1.1]pentane (BCP) and sulfur motifs in pharmaceutical compounds underscores the significance synthesizing suitably functionalized BCP thioethers. In response, we have developed a metal-free photocatalyst-free strategy that harnesses visible light-induced radical cascades. This approach culminates synthesis essential thio-BCP derivatives, which serve as crucial precursors for formation corresponding sulfoxides, sulfones, sulfoximines. Importantly, this methodology exhibits potential large-scale applications, displaying commendable tolerance towards various functional groups while operating under mild reaction conditions.
Язык: Английский
Процитировано
8The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(15), С. 10760 - 10772
Опубликована: Июль 11, 2024
Lewis acid-mediated selective C3-isothiocyanation of quinoxalin-2(1
Язык: Английский
Процитировано
2Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Янв. 1, 2024
The regioselective 1,2-dicarbonylation of aryls and heteroaryls offers access to functionalized dicarbonylated heteroaryls, which opens pharmaceuticals bioactive molecules with diverse synthetic utility.
Язык: Английский
Процитировано
2The Journal of Organic Chemistry, Год журнала: 2023, Номер 88(16), С. 11762 - 11766
Опубликована: Авг. 9, 2023
A metal-free addition of unactivated alkyl bromides to quinoxalin-2(1H)-ones is described. This method enables the construction valuable 3,3-disubstituted dihydroquinoxalin-2(1H)-ones bearing quaternary carbon centers under mild, visible-light photoredox catalysis. High functional group tolerance observed in both quinoxalinone and bromide partners. The ability scale up this was demonstrated photo-flow conditions enable gram-scale synthesis.
Язык: Английский
Процитировано
4New Journal of Chemistry, Год журнала: 2023, Номер 47(47), С. 21596 - 21599
Опубликована: Янв. 1, 2023
Ionic liquid-catalysed oxygenation of quinoxalin-2(1 H )-one utilizing aerobic oxygen as a green oxidant under visible light conditions at room temperature is described.
Язык: Английский
Процитировано
4Asian Journal of Organic Chemistry, Год журнала: 2024, Номер 13(7)
Опубликована: Апрель 17, 2024
Abstract A novel alkenylation reaction between N ‐hydroxyphthalimide (NHPI) esters and alkenyl sulfones is reported. It undergoes the formation of electron donor‐acceptor (EDA) complex a series alkenes are obtained in good to excellent yields. has advantages simple operation, mild conditions, metal‐free.
Язык: Английский
Процитировано
1Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(11), С. 2279 - 2283
Опубликована: Янв. 1, 2024
Here, we demonstrate a practical method toward the facile synthesis of CF
Язык: Английский
Процитировано
1Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(29), С. 5924 - 5929
Опубликована: Янв. 1, 2024
A transition-metal- and photocatalyst-free photochemical acylation strategy driven by the photoexcitation of an electron donor–acceptor (EDA) complex has been developed.
Язык: Английский
Процитировано
1Chemical Communications, Год журнала: 2024, Номер 60(72), С. 9757 - 9760
Опубликована: Янв. 1, 2024
The functionalization of α-C(sp
Язык: Английский
Процитировано
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