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• W1986455925 startingPage "3365" @default.
• W1986455925 abstract "The direct, regioselective, and stereoselective arylation of activated alkynes with aryl iodides using a nickel catalyst and manganese reductant is described. The reaction conditions are mild (40 °C in MeOH, no acid or base) and an intermediate organomanganese reagent is unlikely. Functional groups tolerated include halides and pseudohalides, free and protected anilines, and a benzyl alcohol. Other activated alkynes including an amide and a ketone also reacted to form arylated products in good yields." @default.
• W1986455925 created "2016-06-24" @default.
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• W1986455925 date "2015-06-01" @default.
• W1986455925 modified "2023-09-27" @default.
• W1986455925 title "Nickel-catalyzed reductive arylation of activated alkynes with aryl iodides" @default.
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• W1986455925 doi "https://doi.org/10.1016/j.tetlet.2015.02.120" @default.
• W1986455925 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4446700" @default.
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