1333151-48-6Relevant academic research and scientific papers
Improving the yield of the exhaustive grignard alkylation of n-benzylphthalimide
Jayawardena, Viraj C.,Fairfull-Smith, Kathryn E.,Bottle, Steven E.
, p. 619 - 625 (2013/07/26)
The tetraalkylation of N-benzylphthalimide is the major yield limiting step in the common synthetic route to isoindoline nitroxides. The progress of this reaction was found to be limited by the formation of previously unobserved mono-and dialkyl side prod
N-Capping of primary amines with 2-Acylbenzaldehydes to give isoindolinones
Augner, Daniel,Gerbino, Dario C.,Slavov, Nikolay,Neudoerfl, Joerg-Martin,Schmalz, Hans-Guenther
supporting information; experimental part, p. 5374 - 5377 (2011/12/03)
A unique reactivity pattern, first observed in the conversion of the marine natural product pestalone into pestalachloride A, was investigated. It was shown that 2-formyl-arylketones smoothly react with ammonia and primary amines, respectively, under mild
