Chemical Engineering Journal, Год журнала: 2024, Номер 496, С. 154290 - 154290
Опубликована: Июль 26, 2024
Язык: Английский
Chemical Engineering Journal, Год журнала: 2024, Номер 496, С. 154290 - 154290
Опубликована: Июль 26, 2024
Язык: Английский
Journal of Molecular Structure, Год журнала: 2025, Номер unknown, С. 141375 - 141375
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
5The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 10, 2025
Compared with the well-developed cyclization of functionalized propargylamines, use unactivated tertiary propargylamines to access pyrroles remains challenging. Herein, we report an efficient method for constructing tetrasubstituted via a DBU-mediated intramolecular cycloaddition N-alkyl propargylamines. This reaction employs dihydropyrrole intermediates, followed by oxidation produce in presence 2,3-dichloro-5,6-dicyano-p-benzoquinone. In addition, broad substrate scope, high atom economy, selectivity, and simple operation are also advantages this protocol.
Язык: Английский
Процитировано
1Green Chemistry, Год журнала: 2024, Номер 26(16), С. 9230 - 9240
Опубликована: Янв. 1, 2024
The rapid, eco-friendly, solvent- and metal-free microwave-assisted synthesis of pyrimido[1,2- a ]benzimidazole in high yields was achieved using the green organocatalyst guanidine hydrochloride simple inexpensive starting materials.
Язык: Английский
Процитировано
4Future Medicinal Chemistry, Год журнала: 2025, Номер unknown, С. 1 - 16
Опубликована: Март 3, 2025
Aim This study investigates the anti-proliferative potential and possible molecular mechanisms of 3-(2-furoyl)-indole derivatives against HepG2.
Язык: Английский
Процитировано
0The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(21), С. 16015 - 16021
Опубликована: Окт. 15, 2024
Pyrroles, privileged structural motifs in drug and material science, have been synthesized by indium(III)-catalyzed intramolecular cyclization of homopropargyl azides. This methodology exhibits a broad substrate scope, providing substituted pyrroles bispyrroles good yields. Furthermore, an atom-economical sequential method for the synthesis benzo[
Язык: Английский
Процитировано
1RSC Advances, Год журнала: 2024, Номер 14(22), С. 15713 - 15720
Опубликована: Янв. 1, 2024
A chemoselective one-pot synthesis of indole–pyrrole hybrids has been developed. The new were phenotypically screened for efficacy against L. infantum promastigotes. Compound 3d was the most active with IC 50 = 9.6 μM and a selectivity index 5.
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2024, Номер 496, С. 154290 - 154290
Опубликована: Июль 26, 2024
Язык: Английский
Процитировано
0