REACTION OF 2-SUBSTITUTED 5,5-DIMETHYL-4-OXO-1-PYRROLINE-1-OXIDES WITH NUCLEOPHILIC REAGENTS AND SYNTHESIS OF NITROXYL RADICALS - DERIVATIVES OF PYRROLIDINE

Article abstract of DOI:10.1007/BF00960663

The reaction of β-oxonitrones, derivatives of pyrroline, with nitrogeneous nucleophiles and NaBH4 proceeds at the carbonyl group with the retention of the nitrone group.The reaction with organomagnesium and organolithium compounds takes place at the nitro