
Green Synthesis and Catalysis, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 1, 2024
Language: Английский
Green Synthesis and Catalysis, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 1, 2024
Language: Английский
Advanced Materials, Journal Year: 2024, Volume and Issue: 36(25)
Published: April 2, 2024
Abstract Renewable electricity‐powered nitrate/carbon dioxide co‐reduction reaction toward urea production paves an attractive alternative to industrial processes and offers a clean on‐site approach closing the global nitrogen cycle. However, its large‐scale implantation is severely impeded by challenging C–N coupling requires electrocatalysts with high activity/selectivity. Here, cobalt‐nanoparticles anchored on carbon nanosheet (Co NPs@C) are proposed as catalyst electrode boost yield Faradaic efficiency (FE) electrosynthesis enhanced coupling. Such Co NPs@C renders superb urea‐producing activity FE reaching 54.3% of 2217.5 µg h −1 mg cat. , much superior NPs C counterparts, meanwhile shows strong stability. The affords rich catalytically active sites, fast reactant diffusion, sufficient catalytic surfaces‐electrolyte contacts favored charge ion transfer efficiencies. theoretical calculations reveal that high‐rate formation *CO *NH 2 intermediates crucial for facilitating synthesis.
Language: Английский
Citations
47Organic Letters, Journal Year: 2024, Volume and Issue: 26(18), P. 3727 - 3732
Published: April 28, 2024
Photoexcitation electron donor-acceptor (EDA) complexes provide an effective approach to produce radicals under mild conditions, while the catalytic version of EDA complex photoactivation remains scarce. Herein, we report a visible-light-induced organophotocatalytic pathway for cyanoalkylation azauracils using inexpensive and readily available 1,4-diazabicyclo[2.2.2]octane (DABCO) as donor. This synthetic method exhibits exceptional compatibility with various functional groups presents 34 examples in high yields. The efficient offers environmentally friendly sustainable route toward enhancing structural diversity azauracils.
Language: Английский
Citations
10Chemical Communications, Journal Year: 2024, Volume and Issue: 60(21), P. 2958 - 2961
Published: Jan. 1, 2024
Visible-light-driven EDA complex-promoted ring-opening of cycloketone oxime esters to synthesise various 4-cyanoalkylated isoquinoline-1,3-diones with acryloylbenzamides was developed.
Language: Английский
Citations
9ACS Catalysis, Journal Year: 2024, Volume and Issue: 14(13), P. 10053 - 10059
Published: June 20, 2024
Language: Английский
Citations
8Chemical Science, Journal Year: 2024, Volume and Issue: 15(32), P. 13041 - 13048
Published: Jan. 1, 2024
Herein, a catalytic photoredox-neutral strategy for alkyne deuterocarboxylation with tetrabutylammonium oxalate as the carbonyl source and D
Language: Английский
Citations
4The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 13, 2025
Herein, we report sodium iodide (NaI)-catalyzed decarboxylative C–H alkylation of azauracils with N-hydroxyphthalimide (NHPI) esters facilitated by visible light activation catalytic electron donor–acceptor (EDA) complexes. Control experiments and density functional theory calculations suggest that the coupling reaction proceeds via a transiently assembled EDA complex between NHPI ester NaI in N,N-dimethylacetamide solvent. This synthetic method efficiently applies to primary, secondary, tertiary under mild, photocatalyst-free, redox-neutral conditions, achieving high yields desired alkylated azauracils.
Language: Английский
Citations
0Nature Communications, Journal Year: 2025, Volume and Issue: 16(1)
Published: Feb. 21, 2025
Carboxylation with CO2 offers an attractive and sustainable access to valuable carboxylic acids. Among these methods, direct C−H carboxylation of terminal alkynes has attracted much attention for one-carbon homologation alkynes, enabling rapid synthesis propiolic In contrast, the multi-carbons construct important non-conjugated alkynyl-containing acids not been reported. Herein, we present alkynylcarboxylation alkenes via photoredox copper dual catalysis. This protocol provides a practical method form alkynyl from readily available CO2. Additionally, this approach also features mild (room temperature, 1 atm CO2) redox-neutral conditions, high atom step economy, good functional group tolerance, selectivities. Moreover, diverse transformations β-alkynyl acid products bioactive molecule (GPR40/FFA1 agonist) further illustrate synthetic utility methodology. The report multi-carbon is rare. authors catalysis, affording
Language: Английский
Citations
0Topics in Current Chemistry, Journal Year: 2025, Volume and Issue: 383(1)
Published: March 3, 2025
Language: Английский
Citations
0Organic Letters, Journal Year: 2025, Volume and Issue: unknown
Published: March 24, 2025
A visible-light photocatalytic nucleophilic addition of 4-pyridylphosphonium salts to CO2 and carbonyl compounds is reported. The reaction has mild conditions, good functional group tolerance, a wide range substrates. Mechanistic studies show that the may occur through pyridylphosphonium salt radical anion, pyridyl radical, anion intermediates. By combination with C4-H phosphination, this method can be applied late-stage C-H functionalization drugs containing pyridine unit.
Language: Английский
Citations
0ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 7792 - 7799
Published: April 25, 2025
Language: Английский
Citations
0