ArticleBMC chemistry2022
Visible-light-driven radical Friedländer hetero-annulation of 2-aminoaryl ketone and α-methylene carbonyl compound via organic dye fluorescein through a single-electron transfer (SET) pathway.
Article in BMC chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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1 citing paper in PubMed, 6 citations in OpenAlex.
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1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The discoveries recommend that the photoinduced conditions of fluorescein-determined go about as impetus for photochemically combining polysubstituted quinolines in ethanol at room temperature under air environment by means of revolutionary Friedländer hetero-annulation of 2-aminoaryl ketone and α-methylene carbonyl compound. This study lays out an original capability for photochemically orchestrating fluorescein. This non-metallic organic dye is economically accessible and modest, producing great outcomes, accelerating the cycle, and achieving a high compound economy. The turnover number (TON) and turnover recurrence (TOF) of polysubstituted quinolines have been determined. This cycle will likewise run on a gram scale, demonstrating the chance of modern applications.
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Registered trials
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