Note: This product can be packaged on demand. For information on pricing, availability and packaging of custom sizes, please contact Stable Isotopes Customer Service
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
Journal of the American Chemical Society, 135(4), 1248-1251 (2013-01-15)
Heterolytic splitting of the Si-H bond mediated by a Ru-S bond forms a sulfur-stabilized silicon cation that is sufficiently electrophilic to abstract fluoride from CF(3) groups attached to selected anilines. The ability of the Ru-H complex, generated in the cooperative
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 48(9), 1012-1018 (2013-04-12)
This study was undertaken to investigate the feasibility of applying the Fered-Fenton process to the degradation of m-phenylenediamine, by examining the effect of varying the initial H2O2 and Fe(2+) concentrations, the initial pH and electric current on the process efficiency.
N-substituted indoles are synthesized from primary amines through a tandem reaction sequence. Initial condensation of the amine with an α-(o-haloaryl)ketone or aldehyde is followed by intramolecular aryl amination catalyzed by CuI. A variety of anilines and alkyl amines, including those
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 106, 34-40 (2013-01-30)
For the first time, chemical oxidation of aniline and N-methylaniline with dichromate as oxidant has been studied by Raman spectroscopy with 785 nm laser beam excitation, and the suitability of this technique for kinetic study of this process was demonstrated.
Chemical communications (Cambridge, England), 49(6), 561-563 (2012-12-05)
Two different cyclic amino esters are synthesized by palladium-catalyzed cross-coupling reaction of diazoesters with N-substituted-2-iodoanilines. Aryldiazoacetates lead to cyclic α-amino esters with an α-quaternary carbon centre in the presence of CO. Additionally, arylvinyldiazoacetates afford cyclic α,β-unsaturated γ-amino esters.
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