: In this work, the synthesis of an N-monoarylated dihydrophenazine is reported together with its interconversion to its oxidized mono-cationic form. While the reduced state was employed for the dechlorination of aromatic substrates, the oxidized mono-cationic one was exploited for the formation of C-N bonds between aryl rings and azoles, which was achieved with high yields and very low catalyst loadings (down to 0.5 mol%).
N-Monoarylated dihydrophenazines in reduced and oxidized states as efficient organo-photocatalysts
Prato M.
;Dosso J.
Secondo
2025-01-01
Abstract
: In this work, the synthesis of an N-monoarylated dihydrophenazine is reported together with its interconversion to its oxidized mono-cationic form. While the reduced state was employed for the dechlorination of aromatic substrates, the oxidized mono-cationic one was exploited for the formation of C-N bonds between aryl rings and azoles, which was achieved with high yields and very low catalyst loadings (down to 0.5 mol%).File in questo prodotto:
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