Alfa Chemistry knows that continuous learning is the source of enterprise progress and the fundamental of scientific and technological innovation. We hope to continue to provide you with cutting-edge technologies and products through continuous learning, and also hope to study together with you to contribute to the development of organofluorine chemistry. With this in mind, Alfa Chemistry has shared some of the latest articles related to organofluorine products and technologies and their applications.
LATEST ARTICLES
Synthesis of Fluorinated Compounds by Nickel-Catalyzed Defluorinative Cross-Coupling Reactions (Wang K., et al. ACS Catalysis, 2023, 13: 12238-12268.)
Sulfur-based organofluorine reagents for selective fluorination, fluoroalkylation, and fluoroolefination reactions (Wang X., et al. Phosphorus, Sulfur, and Silicon and the Related Elements, 2023: 1-13.)
Zinc Chelate Complexes of N‐Acyl Hydrazones as Substrates for Addition of Alkyl and Fluorinated Radicals (Rubanov Z., et al. Advanced Synthesis & Catalysis, 2023.)
Trivalent Phosphine‐Catalyzed Reactions Using Fluorinated Building Blocks (Li Y., et al. Advanced Synthesis & Catalysis, 2023.)
Biodegradation of Amphipathic Fluorinated Peptides Reveals a New Bacterial Defluorinating Activity and a New Source of Natural Organofluorine Compounds (Khan M. F., et al. Environmental Science & Technology, 2023.)
Copper-catalysed difluorocarbene transfer enables modular synthesis (Zeng X., et al. Nature Chemistry, 2023: 1-10.)
Radiation-Initiated Dehalogenation of Organofluorine Compounds in Aqueous Solutions (Tugai O. V., et al. High Energy Chemistry, 2023, 57(3): 247-251.)
Recent advances in ionic liquid mediated selective fluorination of organic compounds (Chatterjee R., et al. Journal of Fluorine Chemistry, 2023: 110133.)
Visible light-mediated radical perfluoroalkylation reactions using heterogeneous graphitic carbon nitride (Xiao Y., et al. Journal of Catalysis, 2023, 426: 52-60.)
Synthetic Strategies Towards and Around the CF3S(O) Structural Motif (Romanenko V. D. Current Organic Chemistry, 2023, 27(5): 411-434.)
Recent advances in the strategic incorporation of fluorine into new-generation taxoid anticancer agents (Jayanetti K., et al. Journal of Fluorine Chemistry, 2023: 110106.)
Recent Developments on Synthesis of Organofluorine Compounds Using Green Approaches (Kalar P. L., et al. Current Organic Chemistry, 2023, 27(3): 190-205.)
Catalytic, Regioselective 1,4-Fluorodifunctionalization of Dienes (Yu Y. J., et al. Angewandte Chemie, 2023, 135(1): e202214906.)
Frontispiece: Palladium‐Catalyzed Arylfluorination of Alkenes: A Powerful New Approach to Organofluorine Compounds (Remete A. M., et al. Chemistry–A European Journal, 2022, 28(63): e202286362.)
A machine learning approach for predicting the fluorination strength of electrophilic fluorinating reagents (Saini V. Physical Chemistry Chemical Physics, 2022, 24(43): 26802-26812.)
Benzimidazolium salts bearing the trifluoromethyl group as organofluorine compounds: Synthesis, characterization, crystal structure, in silico study, and inhibitory profiles against acetylcholinesterase and α-glycosidase (Tezcan B., et al. Journal of Biochemical and Molecular Toxicology, 2022, 36(4): e23001.)
S-(Trifluoromethyl)Benzothioate (TFBT): A KF-Based Reagent for Nucleophilic Trifluoromethylthiolation (Meng D., et al. Chemistry–A European Journal, 2022, 28(13): e202104395.)
Electrochemical Trifluoromethoxylation of (Hetero)aromatics with a Trifluoromethyl Source and Oxygen (Ouyang Y., et al. Angewandte Chemie International Edition, 2022, 61(3): e202114048.)
Hypervalent Iodine and Sulfur-Mediated C-H Functionalization (Xu Z., et al. Handbook of CH‐Functionalization, 2022: 1-42.)
Catalytic and Stereoselective Transformations with Easily Accessible and Purchasable Allyl and Alkenyl Fluorides (Paioti P. H. S., et al. Angewandte Chemie, 2022, 134(46): e202208742.)
A Convenient Synthesis of Fluoroalkylated Benzimidazole- or Indole-fused Benzoxazines (Hu Y., et al. European Journal of Organic Chemistry, 2022, 2022(5): e202101501.)
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