Journal of the Iranian Chemical Society, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 4, 2024
Language: Английский
Journal of the Iranian Chemical Society, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 4, 2024
Language: Английский
Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: unknown
Published: Jan. 1, 2024
This study describes a pioneering visible-light-induced phosphine-catalyzed halogen-atom transfer (XAT) strategy that heralds new era in the difunctionalization of [1.1.1]propellane.
Language: Английский
Citations
13Industrial Crops and Products, Journal Year: 2024, Volume and Issue: 222, P. 119738 - 119738
Published: Sept. 27, 2024
Language: Английский
Citations
6Organic Letters, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 19, 2024
A photocatalytic hydroamidomethylation of azobenzenes with N,N-dimethylamides has been developed. Using tetrabutylammonium decatungstate (TBADT) as a photocatalyst, an array and reacted smoothly under visible light irradiation, affording previously unreported N-amidomethyl-N,N′-diarylhydrazines in generally high yields. Mechanistic studies indicate that the reaction is enabled by TBADT-mediated hydrogen atom transfer (HAT) photocatalysis. This work fundamentally different from reported N,N-dimethylformamide azobenzenes.
Language: Английский
Citations
4European Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 1, 2025
Abstract Herein, we explore a visible light‐enabled radical addition for the construction of N‐sulfonyl and N‐acyliminophosphorane using triarylphosphine N‐acylaminopyridinium salts in absence transition metal, photocatalyst, oxidant or base. This method employs PAr 3 as both reaction catalyst to promote generation amidyl via N−N bond cleavage salts, materials preparation products. transformation exhibits abroad substrate scope good functional group compatibility.
Language: Английский
Citations
0Organic Letters, Journal Year: 2025, Volume and Issue: unknown
Published: April 15, 2025
The integration of trifluoroacetyl (CF3CO) groups into organic skeletons is a key research topic in synthetic chemistry given their significant potential to boost biological activity. Despite recent developments strategies for incorporating moiety via radical intermediates, the practical utilization inexpensive and readily available trifluoroacetic acids as sources has not yet been developed. Herein, an electrochemical strategy employed achieve deoxygenative transformation directly with assistance PPh3. obtained radicals are then coupled sulfoximine species, thus enabling synthesis N-trifluoroacetylated sulfoximines. Additionally, other fluorinated alkyl carboxylic acids, including perfluoro-, difluoro-, trifluoromethylcarboxylic can also be efficiently utilized under these conditions, leading corresponding acylated Moreover, trifluoroacetylation drug-based molecules easy execution scale-up experiments highlight applicability this protocol.
Language: Английский
Citations
0Organic Letters, Journal Year: 2025, Volume and Issue: unknown
Published: April 18, 2025
The facile synthesis of N-alkyl-N,N'-diarylhydrazines has been a long-standing challenge. Here, we report photoredox-catalyzed hydroalkylation azobenzenes with alkylboronic acids, which successfully affords diverse N-alkyl-N,N'-diarylhydrazines. With an acridinium salt as the photocatalyst and upon visible light irradiation, broad range acids reacted smoothly in presence Lewis base at ambient temperature. Mechanistic studies revealed that reaction proceeds via generation alkyl radicals is facilitated by photoredox catalysis.
Language: Английский
Citations
0Tetrahedron, Journal Year: 2025, Volume and Issue: unknown, P. 134674 - 134674
Published: April 1, 2025
Language: Английский
Citations
0Beilstein Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 20, P. 1348 - 1375
Published: June 14, 2024
Alkyl and acyl radicals play a critical role in the advancement of chemical synthesis. The generation alkyl by activation C – O bonds using visible-light photoredox catalysis offers mild environmentally benign approach to useful transformations. Alcohols, carboxylic acids, anhydrides, xanthates, oxalates, N -phthalimides, thiocarbonates are some examples precursors that can produce reactive homolysis bond. These then go through variety transformations beneficial for construction synthetic materials otherwise difficult access. This study summarizes current developments use organic photocatalysts, transition-metal catalysts, metallaphotocatalysts driven visible light.
Language: Английский
Citations
3Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(20), P. 5876 - 5883
Published: Jan. 1, 2024
A visible-light-induced copper-catalyzed regiodivergent sulfonylation of oxime esters with sodium sulfinates under mild conditions is reported, yielding a range useful β-ketosulfones and sulfonated pyrrolines convertible functional groups.
Language: Английский
Citations
1Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: unknown
Published: Jan. 1, 2024
We present a novel visible light-promoted regiodivergent cyclization, enabling the selective synthesis of distinct azapolyaromatic regioisomers from 2-alkynlazobenzenes.
Language: Английский
Citations
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