248595-18-8Relevant articles and documents
Ruthenium-catalyzed intramolecular selective halogenation of O-methylbenzohydroximoyl halides: A new route to halogenated aromatic nitriles
Chinnagolla, Ravi Kiran,Pimparkar, Sandeep,Jeganmohan, Masilamani
supporting information, p. 3146 - 3148 (2013/06/04)
The intramolecular halogenation of O-methylbenzohydroximoyl halides in the presence of a Ru catalyst and the ligand diphenylacetylene afforded halo substituted aromatic nitriles in a highly regioselective manner. Further, substituted nitriles were converted into substituted tetrazole derivatives in the presence of NaN3 and I2.
Oxidative degradation of arylfuro-1,2-oxazoles to arylnitriles by potassium permanganate
Salgado-Zamora, Hector,Campos, Elena,Jimenez, Rogelio,Ruiz, Rosalba,Castaneda, Teresa,Turijan, Sara
, p. 209 - 212 (2007/10/03)
Arylfuroisoxazolines are oxidatively degraded to arylnitriles by treatment with a mixture of potassium permanganate and sodium acetate in dry dioxane.