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Published in 2017 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.7b05981
Abstract: An Fe(III)-promoted oxidative annulation reaction was developed for the synthesis of 1,2-naphthoquinones. A variety of substituted arylglyoxals and internal alkynes undergo the transformation in the presence of FeCl3 at room temperature to afford the 1,2-naphthoquinone…
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Keywords:
oxidative annulation;
addition;
arylglyoxal alkyne;
promoted oxidative ... See more keywords