Selective Radical-Type Perfluoro-tert-butylation with a Stable Reagent

Introducing a breakthrough in fluorine chemistry: a stable and scalable reagent for efficient perfluoro-tert-butylation, enabling precise control over E/Z selectivity in unsaturated compounds through innovative photocatalysis.

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Key Advantages

Enhanced Selectivity

Achieve remarkable E/Z selectivity in perfluoro-tert-butylation of styrenes through a controllable triplet-triplet energy transfer (TTET) process, a significant leap from traditional methods.

Scalable and Stable Reagent

Utilize a synthesized hypervalent iodine(III) reagent derived from perfluoro-tert-butanol that is both stable and scalable, facilitating its use in large-scale chemical production.

Versatile Synthetic Platform

Leverage a broad synthetic platform for the perfluoro-tert-butylation of unsaturated compounds, including alkenes, alkynes, and electron-rich aromatics, expanding the scope of fluorine chemistry.

Key Applications

Pharmaceutical Intermediates

Explore the use of perfluoro-tert-butanol in the synthesis of complex pharmaceutical intermediates, leveraging its unique chemical properties for drug discovery.

Magnetic Resonance Imaging (MRI)

Discover the role of PFtB-containing compounds in high-performance fluorine-19 MRI agents, enhancing diagnostic capabilities through superior imaging properties.

Material Science

Investigate the incorporation of the perfluoro-tert-butyl group into advanced materials, tailoring properties for specific technological applications.

Agrochemicals

Utilize perfluoro-tert-butylation strategies to develop novel agrochemicals with improved efficacy and stability.