Electrophilic Arylation of Phenols

1-Methyl-3,6,8-trinitro-2-quinolone was found to be a suitable substrate for electrophilic arylation on benzene rings leading to (1,2-dihydro-4-quinolyl)phenols. The resultant products constitute a new family of 1-methyl-2-quinolones, which is often found in biologically active compounds as a partia...

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Published in:Bulletin of the Chemical Society of Japan 2005-12, Vol.78 (12), p.2235
Main Authors: Asahara, Motoki, Ohtsutsumi, Masaki, Tamura, Mina, Nishiwaki, Nagatoshi, Ariga, Masahiro
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container_title Bulletin of the Chemical Society of Japan
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creator Asahara, Motoki
Ohtsutsumi, Masaki
Tamura, Mina
Nishiwaki, Nagatoshi
Ariga, Masahiro
description 1-Methyl-3,6,8-trinitro-2-quinolone was found to be a suitable substrate for electrophilic arylation on benzene rings leading to (1,2-dihydro-4-quinolyl)phenols. The resultant products constitute a new family of 1-methyl-2-quinolones, which is often found in biologically active compounds as a partial structure.
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title Electrophilic Arylation of Phenols
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