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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c00829
Abstract: A palladium-catalyzed cyanation of aryl dimethylsulfonium salts using cheap, nontoxic, and bench-stable K4[Fe(CN)6]·3H2O as the cyanating reagent has been developed. The reactions proceeded well under base-free conditions with various sulfonium salts and provided aryl nitrile…
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Keywords:
cyanation aryl;
catalyzed cyanation;
palladium catalyzed;
sulfonium salts ... See more keywords
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0
Published in 2019 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.9b11208
Abstract: Herein, we report a Ni-catalyzed reductive coupling for the synthesis of benzonitriles from aryl (pseudo)halides and an electrophilic cyanating reagent, 2-methyl-2-phenyl malononitrile (MPMN). MPMN is a bench-stable, carbon-bound electrophilic CN reagent that does not release…
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Keywords:
catalyzed reductive;
cyanation aryl;
aryl halides;
reductive cyanation ... See more keywords
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1
Published in 2017 at "Chemistry Letters"
DOI: 10.1246/cl.170798
Abstract: The copper-catalyzed cyanation of aryl iodides is described using nitromethane as a CN source. In situ generation of a “CN” species from nitromethane is plausible. This strategy is an advantageous synthetic method for the construction…
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Keywords:
aryl iodides;
cyanation aryl;
using nitromethane;
cyanation ... See more keywords