The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(15), P. 10831 - 10843
Published: July 11, 2024
Direct construction of
Language: Английский
The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(15), P. 10831 - 10843
Published: July 11, 2024
Direct construction of
Language: Английский
Chem Catalysis, Journal Year: 2024, Volume and Issue: 4(5), P. 100945 - 100945
Published: March 5, 2024
Language: Английский
Citations
14Chemical Communications, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
In this study, a straightforward and environmentally benign electrochemical mono-functionalization of alkenes has been established for the synthesis alkenyl selenium sulfonates using elemental as source.
Language: Английский
Citations
1Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: 42(19), P. 2346 - 2350
Published: May 27, 2024
Comprehensive Summary Catalytic and green strategies for the synthesis of privileged scaffolds are synthetically appealing. We now report a radical‐polar crossover (RPC)‐enabled three‐component cyclization bromodifluoroalkyls with enaminones 6‐aminouraciles via visible‐light‐induced domino cyclization. The reaction exhibited broad substrate scope (> 40 examples) including complex molecules, which highlighted utility this strategy construction library bioactive analogs.
Language: Английский
Citations
7Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: 42(9), P. 957 - 962
Published: Jan. 18, 2024
Comprehensive Summary Multicomponent alkene 1,2‐dicarbofunctionalizations (DCFs) have emerged as a powerful strategy to rapidly incorporate both two carbon subunits across one C—C double bond in step for enhancing molecular complexity and diversity. To the best of our knowledge, there is only report on photoredox‐catalyzed three‐component DCFs with malonates through radical−radical cross‐coupling, while radical‐polar crossover (RPC)‐type were still rare. Herein, we describe redox‐neutral RPC‐type 1,2‐dialkylation styrenes aldehydes synergistic Brønsted base/photoredox catalysis system. This transition‐metal‐free provides an efficient clean approach broad variety δ‐hydroxy esters also features exceptionally mild conditions, wide compatibility substrate scope functional groups, high atomic economy. Moreover, 1,2‐alkylacylation from same starting materials was achieved one‐pot manner such coupling subsequent two‐electron oxidation process, providing set δ‐keto interest pharmaceutical research.
Language: Английский
Citations
5Chemical Science, Journal Year: 2024, Volume and Issue: 15(27), P. 10659 - 10667
Published: Jan. 1, 2024
The direct activation of α-halo carboxylic acids using visible-light-mediated photoredox catalysis facilitates the formation bifunctional radical intermediates, allowing reactivity toward olefins to be fine-tuned by varying solvent system.
Language: Английский
Citations
5Chinese Journal of Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 16, 2025
Comprehensive Summary Herein, we report a photo‐induced, metal‐/additive‐free protocol for the difluoromethylation of N ‐heteroaromatics with [bis(difluoroacetoxy)iodo]benzene as reagent. The affords difluoromethylated in moderate to good yield (up 91%). transformation is compatible wide range substrates and has tolerance towards various functional groups. Moreover, synthetic value this method further demonstrated by applications gram‐scale synthesis late‐stage functionalization biologically important molecules.
Language: Английский
Citations
0Green Synthesis and Catalysis, Journal Year: 2025, Volume and Issue: unknown
Published: April 1, 2025
Language: Английский
Citations
0Chinese Journal of Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: April 25, 2025
Comprehensive Summary A one‐pot transformation of aliphatic and aromatic tertiary amines to novel fluorinated enaminones has been developed, utilizing perfluoroalkyl ether carboxylates (PFECA salts) featuring “–CF 2 O–” units as the fluorine‐containing reagents. Carbonyl fluoride, acyl fluorides anhydrides by thermal decomposition these PFECA salts were proposed act key active species that trigger tandem oxidation–acylation process amines, through enamine intermediates.
Language: Английский
Citations
0The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(15), P. 10831 - 10843
Published: July 11, 2024
Direct construction of
Language: Английский
Citations
1