106073-17-0Relevant articles and documents
Ring Size and Substitution Effects in the Tandem Reduction-Lactamization of ortho-Substituted Nitroarenes
Nammalwar, Baskar,Bunce, Richard A.,Hiett, John T.
, p. 338 - 355 (2015)
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Preparation electrochimique de derives de la quinoleine. II. Electroreduction d'o-nitrobenzylidenes substitues
Chibani, A.,Hazard, R.,Jubault, M.,Tallec, A.
, p. 795 - 802 (2007/10/02)
Quinoline N-oxydes and N-hydroxyquinolones have been prepared by controlled potential electrolysis of o-nitrobenzylidenes: o-NO2-C6H4-CH=CX2, o-NO2-C6H4-CH=CRX, o-NO2-C6H4-CH=CXY (X and Y being electron withdrawing groups: CO2Et, CN, CONH2, COPh).As a gen