Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(11), P. 3321 - 3321
Published: Jan. 1, 2024
Language: Английский
Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(11), P. 3321 - 3321
Published: Jan. 1, 2024
Language: Английский
Organic Letters, Journal Year: 2024, Volume and Issue: 26(34), P. 7139 - 7143
Published: Aug. 15, 2024
We report an efficient perfluoroalkoxylation reaction of alkyl halides catalyzed by copper(I) iodide (CuI), which facilitates the simultaneous activation both perfluoroalkoxide and halides. This methodology is tolerant a wide range functional groups eliminates need for costly metal reagents. The conducted in single step under mildly practical conditions.
Language: Английский
Citations
1Organic Letters, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 5, 2024
We present a straightforward method for the synthesis of Ngai trifluoromethoxy reagent and longer carbon chain variants, thereby expanding range options perfluoroalkoxylation reactions. Utilizing cost-effective sodium perfluoroalkane sulfinates (R
Language: Английский
Citations
1Synlett, Journal Year: 2023, Volume and Issue: 35(03), P. 268 - 278
Published: July 18, 2023
Abstract We report herein recent advances made by our group and others in the field of oxygen-centered radicals generated under photocatalysis. Thanks to design new O-radical precursors, these can now be efficiently trapped unsaturated systems an intermolecular manner, via formation a C–O bond. 1 Introduction 2 Reactions Involving Carbonyloxy Radicals 3 Fluoroalkoxy 4 Alkoxy 5 Conclusion
Language: Английский
Citations
2Angewandte Chemie, Journal Year: 2024, Volume and Issue: 136(40)
Published: June 20, 2024
Abstract The 2,2‐difluoroethyl group is an important lipophilic hydrogen bond donor in medicinal chemistry, but its incorporation into small molecules often challenging. Herein, we demonstrate electrophilic 2,2‐difluoroethylation of thiol, amine and alcohol nucleophiles with a hypervalent iodine reagent, (2,2‐difluoro‐ethyl)(aryl)iodonium triflate, via proposed ligand coupling mechanism. This transformation offers complementary strategy to existing methods allows access wide range 2,2‐difluoroethylated nucleophiles, including the drugs Captopril, Normorphine Mefloquine.
Language: Английский
Citations
0Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(7), P. 2174 - 2174
Published: Jan. 1, 2024
Language: Английский
Citations
0Synlett, Journal Year: 2024, Volume and Issue: unknown
Published: July 31, 2024
Abstract In recent years, there have been increasing efforts in the development of methodologies for incorporating fluorine-containing functional groups into organic scaffolds. Modern techniques made fluorinated molecules more accessible than ever before, but many fluorination reactions still limitations their generality, predictability, sustainability, and cost-effectiveness. The methodological progress has a significant impact on drug discovery materials science research. Photoredox catalysis enabled effective methods, providing access to druglike molecules. Photochemical methods paired with C–H functionalization provide powerful tools property-driven Herein, we examine developments at interface photoredox functionalization. 1 Introduction 2 Fluorinations 3 Fluoroalkylations 4 Fluoroalkoxylations 5 Conclusion
Language: Английский
Citations
0Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(11), P. 3321 - 3321
Published: Jan. 1, 2024
Language: Английский
Citations
0