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- W3100656239 endingPage "29863" @default.
- W3100656239 startingPage "29854" @default.
- W3100656239 abstract "A comfortable, environment-friendly, and metal-free approach for synthesizing the biologically important moiety aminoimidazopyridine through the multicomponent reaction of benzylamine, 2-aminopyridine, and t-butyl isocyanide under visible light using eosin Y as a photocatalyst has been developed. Inexpensive, nontoxic, the effortless accessibility of starting materials, and nonparticipation of particular glassware and a photoreactor system are important qualities of the current approach. Strangely, the mild conditions, environment-friendly, and enumerating tolerance of an extensive range of both electron-donating and electron-withdrawing groups are additional features of the approach." @default.
- W3100656239 created "2020-11-23" @default.
- W3100656239 creator A5027275035 @default.
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- W3100656239 date "2020-11-12" @default.
- W3100656239 modified "2023-10-17" @default.
- W3100656239 title "Eosin Y-Catalyzed Synthesis of 3-Aminoimidazo[1,2-<i>a</i>]Pyridines via the HAT Process under Visible Light through Formation of the C–N Bond" @default.
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- W3100656239 doi "https://doi.org/10.1021/acsomega.0c03941" @default.
- W3100656239 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7689671" @default.
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- W3100656239 hasPublicationYear "2020" @default.
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