117911-80-5Relevant articles and documents
PIII/PV═O-Catalyzed Intermolecular N-N Bond Formation: Cross-Selective Reductive Coupling of Nitroarenes and Anilines
Li, Gen,Miller, Steven P.,Radosevich, Alexander T.
supporting information, p. 14464 - 14469 (2021/09/18)
An organophosphorus-catalyzed method for the synthesis of unsymmetrical hydrazines by cross-selective intermolecular N-N reductive coupling is reported. This method employs a small ring phosphacycle (phosphetane) catalyst together with hydrosilane as the terminal reductant to drive reductive coupling of nitroarenes and anilines with good chemoselectivity and functional group tolerance. Mechanistic investigations support an autotandem catalytic reaction cascade in which the organophosphorus catalyst drives two sequential and mechanistically distinct reduction events via PIII/PV═O cycling in order to furnish the target N-N bond.
HYDRAZINES AND AZO COMPOUNDS FROM O-DIPHENYLPHOSPHINOYL ARYLHYDROXYLAMINES
Boche, Gernot,Meier, Chris,Kleemiss, Wolfgang
, p. 1777 - 1780 (2007/10/02)
The reactions of the O-diphenylphosphinoylhydroxylamines 1a-d with the amines 2-4 lead to the hydrazines 5 and the symmetrical azo compounds 6. 5 are formed via electrophilic amination; the azo compounds 6 do not result from the corresponding phenylnitrene intermediates.