Search results for "Ferricyanide"
showing 2 items of 12 documents
Relationship between Auxin-Dependent Proton Extrusion and Plasmalemma Redox System in Maize Coleoptile Segments
1988
Abraded coleoptile segments reduce ferricyanide utilizing endogenous substrates. The kinetics of ferricyanide reduction shows an initial rapid rate followed by a slow rate of reduction. The duration of the initial phase is about 5 minutes. The slow phase is observed for more than 30 minutes. A Lineweaver-Burk plot of the slow phase was linear and revealed maximum velocity of the reaction of 42 nmols ferricyanide reduced/hour*coleoptile segment and an apparent Km (ferri) of 2.25mM.
ChemInform Abstract: α-Cyanation of Aromatic Tertiary Amines Using Ferricyanide as a Non-Toxic Cyanide Source.
2016
Aromatic tertiary amines, mostly isoquinoline derivatives and analogous N-heterocycles, are treated with the non-toxic agent (II) under conditions A) or B) to produce the desired N-aminonitrile compounds as amino acid precursors and as building blocks of complex nitrogen heterocycles.