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Access to SCF3 substituted indolizines via a photocatalytic late-stage functionalization protocol

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NIAID Data Ecosystem2026-05-02 收录
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http://datadryad.org/dataset/doi%253A10.5061%252Fdryad.v6wwpzh7x
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A mild, scalable, and highly chemoselective photocatalytic method was developed for the direct indolizine functionalization with N-((trifluoromethyl)thio)saccharin, yielding high amounts of desired products while tolerating various functional groups. The photoredox catalyst employed offers a straightforward and inexpensive alternative to commercially available catalysts. Additionally, a 3-SCF₃ analogue of a histamine H3 receptor antagonist was synthesized with excellent yield, demonstrating the strategy’s potential in developing biologically relevant molecules. Methods All NMR-Data FID files were recorded by either a BRUKER Digital AVANCE 400 MHz FT-NMR or a BRUKER Digital AVANCE III 600 MHz FT-NMR.
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2025-07-31
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