80585-16-6Relevant articles and documents
Efficient Additions of an Electronically Stabilized Persistent Aminyl Radical to Conjugated Alkenes
Miura, Yozo,Kunishi, Teruo,Kinoshita, Masayoshi
, p. 1696 - 1698 (1985)
It has been found that an electronically stabilized persistent N-(4-chlorophenylthio)-3,5-di-t-butyl-phenylaminyl radical (1) adds to conjugated alkenes to afford 1:2 adducts of the alkenes and 1 in fair to excellent yields, along with small amounts of 1:
Persistent Nitrogen-centered Free Radicals, N-(Arylthio)-3,5-di-t-butylphenylaminyls. Decomposition Reactions
Miura, Yozo,Yamamoto, Akifumi,Kinoshita, Masayoshi
, p. 3215 - 3216 (2007/10/02)
N-(4-Chlorophenylthio)-3,5-di-t-butylphenylaminyl was decomposed in oxygen-free benzene, and the products were examined.On the basis of the results, the decomposition mechanism of the radical is described.