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- W2168249441 abstract "Abstract A series of 2-( S )-isopropyl-pyrimidinones functionalized at C5 with triazole rings, in which the substituents are found at N-1′ of the triazole ring, were synthesized. Through the azide–acetylene cycloaddition reaction, using CuI as a copper source and ultrasonic waves as an energy source it was possible to obtain products with yields ranging from 79% to 89% within 5 min or less. A preliminary study to gain further insight into the reaction was performed using in situ ReactIR technology." @default.
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- W2168249441 date "2011-12-01" @default.
- W2168249441 modified "2023-10-17" @default.
- W2168249441 title "Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through Cu(I)-mediated 1,3-dipolar azide–alkyne cycloadditions" @default.
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- W2168249441 doi "https://doi.org/10.1016/j.tetlet.2011.10.011" @default.
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