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• W2075306971 abstract "Carbonated analogues of ribavirin were synthesized from ethyl C-ribosylpropiolate obtained by an alkynylation reaction mediated by indium(0). The C-ribosides were then engaged in a Huisgen 1,3-dipolar cycloaddition reaction under a micellar catalysis. In these conditions, formation of 1,2,3-triazoles with control of the regioselectivity was observed. The regiochemistry of the adducts was determined by HMBC 2D-NMR analysis." @default.
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• W2075306971 date "2009-05-13" @default.
• W2075306971 modified "2023-10-18" @default.
• W2075306971 title "Huisgen Cycloaddition Reaction of <i>C</i>-Alkynyl Ribosides under Micellar Catalysis: Synthesis of Ribavirin Analogues" @default.
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• W2075306971 doi "https://doi.org/10.1021/jo900594x" @default.
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