Опубликована: Янв. 1, 2024
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Язык: Английский
Опубликована: Янв. 1, 2024
Download This Paper Open PDF in Browser Add to My Library Share: Permalink Using these links will ensure access this page indefinitely Copy URL DOI
Язык: Английский
ACS Catalysis, Год журнала: 2023, Номер 13(22), С. 15013 - 15053
Опубликована: Ноя. 6, 2023
Methanol is a fundamental feedstock and widely used in the chemical petroleum industries. It can serve as C1 source to make variety of C–C C–N bond formation dehydrogenative coupling products, which have important applications natural products drug discovery. A high hydrogen content (12.5 wt%) methanol makes it an effective H2 donor for transfer hydrogenation various reducible functional groups. plethora transition metal-based processes been developed using methanol. Notably, recent review articles focused on aspect However, more updated that examines challenges both C1-source H2-source organic transformations contributing concept economy has not presented yet. This Review summarizes (homogeneous, heterogeneous, photo-) catalyst system C-, N-, O-methylation ketones, alcohols, amides, nitriles, heterocyclic compounds, sulfones, amines, sulfonamides direct N-methylation nitro compounds under borrowing strategy N-formylation amines acceptorless dehydrogenation source. also covers insights into reaction mechanisms role carefully selected ligands metal catalysis activation incorporation -CD3, methylation molecules. Moreover, describes groups such aldehydes, alkynes, with detail.
Язык: Английский
Процитировано
31Journal of Colloid and Interface Science, Год журнала: 2023, Номер 657, С. 449 - 462
Опубликована: Ноя. 28, 2023
Язык: Английский
Процитировано
30Green Chemistry, Год журнала: 2024, Номер 26(6), С. 3021 - 3038
Опубликована: Янв. 1, 2024
Production of value-added chemicals from renewable feedstocks is an attractive platform to alleviate the shortage petroleum resources and minimize CO 2 emissions.
Язык: Английский
Процитировано
10Organic Letters, Год журнала: 2024, Номер 26(4), С. 866 - 871
Опубликована: Янв. 25, 2024
In this study, we report a transfer hydrogenation protocol that utilizes borane–ammonia (H3N–BH3) as the hydrogen source and commercially available RuCl3·xH2O precatalyst for selective aromatic reduction of quinolines, quinoxalines, pyridines, pyrazines, indoles, benzofurans, furan derivatives to form corresponding alicyclic heterocycles in good excellent isolated yields. Applications straightforward include efficient preparation useful key pharmaceutical intermediates, such donepezil flumequine, including biologically active compound.
Язык: Английский
Процитировано
9ACS Sustainable Chemistry & Engineering, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 28, 2024
It is a great challenge to construct green catalytic system for the reduction of nitro compounds corresponding amines under mild conditions. Due low energy red light, it challenging develop photocatalytic selective nitroaromatics aromatic driven by light. A bimetallic porphyrin metal–organic framework (Bi-P(Co)MOF) was characterized Fourier transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy, scanning and energy-dispersive techniques. The constructed photocatalyst Bi-PMOF-Co shows excellent activity conversion in high yields with NaBH4 as reducing agent at room temperature light irradiation. Moreover, protocol showed functional group compatibility, recyclability demonstrated five-cycle tests.
Язык: Английский
Процитировано
9Journal of Catalysis, Год журнала: 2024, Номер 438, С. 115685 - 115685
Опубликована: Авг. 3, 2024
Язык: Английский
Процитировано
5Journal of Catalysis, Год журнала: 2024, Номер 434, С. 115506 - 115506
Опубликована: Апрель 20, 2024
Язык: Английский
Процитировано
4ACS Sustainable Chemistry & Engineering, Год журнала: 2024, Номер 12(19), С. 7644 - 7654
Опубликована: Апрель 30, 2024
A direct and efficient synthesis of N-methyl-1,2,3,4-tetrahydroquinolines (MTHQs) is achieved through the one-pot reductive N-methylation quinolines. The SnOx-decorated Pt/Al2O3 (Pt-SnOx/Al2O3) catalyst proves to be highly effective in transformation from quinolines MTHQs, using methanol as exclusive source for hydrogen (H) methyl (CH3), without addition additional bases or additives. Mechanistic kinetic studies reveal a tandem reaction pathway: (1) dehydrogenation methanol, (2) reduction 1,2,3,4-tetrahydroquinolines (THQs), (3) THQs with identified rate-determining step. Characterization catalytic performance results demonstrate that SnOx modifies morphology electronic properties Pt-based metal active sites, which dramatically facilitates cleavage O–H less reactive C–H bonds maintains delicate balance between quinolines, thus obtaining high reactivity total transformation.
Язык: Английский
Процитировано
4Chemical Communications, Год журнала: 2023, Номер 59(99), С. 14709 - 14712
Опубликована: Янв. 1, 2023
Homogeneous Ni-catalyzed highly selective transfer hydrogenation of nitroarenes was successfully established using NH3BH3 as a hydrogen source. A broad range functional groups were selectively reduced to provide the corresponding anilines in good high yields. Further, pharmaceutically active compounds can be prepared that would otherwise challenging access.
Язык: Английский
Процитировано
9CHINESE JOURNAL OF CATALYSIS (CHINESE VERSION), Год журнала: 2024, Номер 58, С. 168 - 179
Опубликована: Март 1, 2024
Язык: Английский
Процитировано
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