24093-23-0Relevant articles and documents
A De Novo Heterodimeric Due Ferri Protein Minimizes the Release of Reactive Intermediates in Dioxygen-Dependent Oxidation
Chino, Marco,Leone, Linda,Maglio, Ornella,D'Alonzo, Daniele,Pirro, Fabio,Pavone, Vincenzo,Nastri, Flavia,Lombardi, Angela
supporting information, p. 15580 - 15583 (2017/11/20)
Metalloproteins utilize O2 as an oxidant, and they often achieve a 4-electron reduction without H2O2 or oxygen radical release. Several proteins have been designed to catalyze one or two-electron oxidative chemistry, but t
Molecular-Level Insight into the Differential Oxidase and Oxygenase Reactivities of de Novo Due Ferri Proteins
Snyder, Rae Ana,Butch, Susan E.,Reig, Amanda J.,DeGrado, William F.,Solomon, Edward I.
supporting information, p. 9302 - 9314 (2015/08/18)
Using the single-chain due ferri (DFsc) peptide scaffold, the differential oxidase and oxygenase reactivities of two 4A→4G variants, one with two histidines at the diiron center (G4DFsc) and the other with three histidines (3His-G4DFsc(Mut3)), are explore
Benzoquinone Imines. Part 18. Kinetics and Mechanism of Oxidative Coupling Reactions involving N,N-bis-(2-hydroxyethyl)-p-phenylenediamine
Palling, David J.,Brown, Keith C.,Corbett, John F.
, p. 65 - 68 (2007/10/02)
A kinetic and mechanistic study of oxidative coupling reactions of N,N-bis-(2-hydroxyethyl)-p-phenylenediamine with m-phenylenediamines, phenols, and acetoacetanilide is described.The reactions involve the rapid establishment of an equilibrium between N,N
