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- W2297625334 abstract "A series of 4-(het)aryl-pyrrolo[2,3-<i>d</i>]pyrimidines [6-(het)aryl-7-deazapurine bases] bearing a H, NH<sub>2</sub>, CH<sub>3</sub>, F, or Cl group at the 2-position and either H or F at the 5-position (position 7 of 7-deazapurine) were prepared in a single step by the aqueous Suzuki–Miyaura cross-coupling reactions of the corresponding 6-chloro-7-deazapurines with (het)arylboronic acids. Unlike their ribonucleoside derivatives, which are potent cytostatics, the deazapurine bases did not show significant biological activity but most of them exerted bright fluorescence with emission maxima 368–468 nm and high quantum yields up to 0.83." @default.
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- W2297625334 date "2016-01-11" @default.
- W2297625334 modified "2023-10-16" @default.
- W2297625334 title "Synthesis of Fluorescent 2-Substituted 6-(Het)aryl-7-deazapurine Bases {4-(Het)aryl-pyrrolo[2,3-d]pyrimidines} by Aqueous Suzuki–Miyaura Cross-Coupling Reactions" @default.
- W2297625334 doi "https://doi.org/10.1055/s-0035-1561287" @default.
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