128792-10-9Relevant articles and documents
Reaction of indolinonic aminoxyls with nitric oxide
Damiani, Elisabetta,Greci, Lucedio,Rizzoli, Corrado
, p. 1139 - 1144 (2001)
2-Methyl-2-phenyl-3-oxoindolin-1-yloxyl and 2-methyl-2-phenyl-3-aryliminoindolin-1-yloxyl radicals react with nitric oxide in the absence and presence of oxygen to form both substituted and unsubstituted N-nitro and N-nitroso stable compounds as the main
Reactions of an indolinonic nitroxide with superoxide radical anion in the presence of alkylhalides. Unexpected formation of a reduced transposed product
Carloni, Patricia,Vianelli, Roberto,Greci, Lucedio
, p. 459 - 464 (2003)
This study concerns the reactions of 2-methyl-2-phenyl-3-phenylimino-2,3-dihydroindol-1-oxyl and 2,2,6,6-tetramethylpiperidine-1-oxyl with alkylperoxyls, generated from potassium superoxide and a series of alkylhalides, in order to evaluate possible differences in reactivity with primary, secondary and tertiary alkylperoxyls. To better understand the reactivity of the studied indolinonic aminoxyl in alkaline medium, the investigation was extended to its reactions with potassium hydroxide and potassium tert-butoxide in different solvents.
HOMOLYTIC SUBSTITUTIONS IN INDOLINONE NITROXIDE RADICALS. V. REACTION WITH tert-BUTYLPEROXY RADICALS
Cardellini, Liberato,Carloni, Patricia,Greci, Lucedio,Stipa, Pierluigi,Faucitano, Antonio
, p. 621 - 626 (2007/10/02)
Indolinone and phenyliminoindolinone nitroxides (3) react with tert-butylperoxy radical to form mono-(4 and 5) and di-substituted (6) tert-butoxyindolinone nitroxides, the quinoneimine N-oxides 7 and 8 and the corresponding tert-butoxy-substituted 9 and 1
