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- W2059563957 endingPage "2103" @default.
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- W2059563957 abstract "The commercially available 2,2′-dipyridylamine was used as a supporting ligand in the palladium-catalyzed Sonogashira cross-coupling reaction. The reactions between aryl iodides and terminal alkynes with different steric hindrance can be efficiently performed in the absence of copper in neat water at room temperature. The superior catalytic performance of the catalytic system was attributed to water solubility of the palladium 2,2′-dipyridylamine complex. Palladium nanoparticles with small size and narrow size distribution were formed after the cross-coupling reaction." @default.
- W2059563957 created "2016-06-24" @default.
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- W2059563957 date "2014-01-01" @default.
- W2059563957 modified "2023-09-27" @default.
- W2059563957 title "The copper-free Sonogashira cross-coupling reaction promoted by palladium complexes of nitrogen-containing chelating ligands in neat water at room temperature" @default.
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- W2059563957 doi "https://doi.org/10.1039/c3dt52970c" @default.
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