92847-23-9Relevant academic research and scientific papers
A mild, ferrocene-catalyzed C-H imidation of (hetero)arenes
Foo, Klement,Sella, Eran,Thomé, Isabelle,Eastgate, Martin D.,Baran, Phil S.
supporting information, p. 5279 - 5282 (2014/05/06)
A simple method for direct C-H imidation is reported using a new perester-based self-immolating reagent and a base-metal catalyst. The succinimide products obtained can be easily deprotected in situ (if desired) to reveal the corresponding anilines directly. The scope of the reaction is broad, the conditions are extremely mild, and the reaction is tolerant of oxidizable and acid-labile functionality, multiple heteroatoms, and aryl iodides. Mechanistic studies indicate that ferrocene (Cp2Fe) plays the role of an electron shuttle in the decomposition of the perester reagent, delivering a succinimidyl radical ready to add to an aromatic system.
A simple key for benzylic mono- and gem-dibromination of primary aromatic amine derivatives using molecular bromine1
Kar, Anirban,Argade, Narshinha P.
, p. 221 - 224 (2007/10/03)
Quantitative benzylic mono- and gem-dibromination on primary aromatic amine derivatives have been achieved using molecular bromine and by protecting the amino group as a succinimide moiety. The reactions of N-(o/m/p-tolyl)succinimides 5a-c with 1.25 equiv
