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CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III
(2013-07-01)
This work describes the mutagenic response of Sudan III, an adulterant food dye, using Salmonella typhimurium assay and the generation of hazardous aromatic amines after different oxidation methods of this azo dye. For ...
CYP-450 isoenzymes catalyze the generation of hazardous aromatic amines after reaction with the azo dye Sudan III
(2013-07-01)
This work describes the mutagenic response of Sudan III, an adulterant food dye, using Salmonella typhimurium assay and the generation of hazardous aromatic amines after different oxidation methods of this azo dye. For ...
Intra- vs inter-molecular electron transfer processes in C[sbnd]N bond forming reactions. Photochemical, photophysical and theoretical study of 2′-halo-[1,1′-biphenyl]-2-amines
(Pergamon-Elsevier Science Ltd, 2016-12)
N-Arylation reaction is obtained when 2′-halo-[1,1′-biphenyl]-2-amines are irradiated in basic medium. On the basis of photochemical, photophysical experiments and computational studies we propose that carbazoles are formed ...
"Transition-metal-free" synthesis of carbazoles by photostimulated reactions of 2′-halo[1,1′-biphenyl]-2-amines
(American Chemical Society, 2014-12)
An efficient and simple protocol for the preparation of a series of 9H-carbazoles by photostimulated SRN1 substitution reactions is presented. Substituted 9H-carbazoles were synthesized in low to excellent yields (up to ...