33925-43-8Relevant articles and documents
Solvatochromic and quantum chemical investigations of newly synthesized succinimides: Substituent effect on intramolecular charge transfer
Banjac, Neboj?a,Tri?ovi?, Nemanja,Vitnik, ?eljko,Vitnik, Vesna,Valenti?, Nata?a,U??umli?, Gordana,Jurani?, Ivan
, p. 1525 - 1535 (2013/10/22)
Two series of 1-aryl-3-phenyl- and 1-aryl-3,3-diphenylpyrrolidine-2,5- diones were synthesized and their solvatochromic properties were studied in a set of 15 solvents of different polarity. The effect of specific and non-specific solvent-solute interacti
Condensed heterocyclic compounds, their production and use
-
, (2008/06/13)
The compound STR1 wherein ring A represents a benzene ring; Ar represents an aromatic group; R 1 and R 2 independently represent hydrogen, acyl or hydrocarbon group or R 1 and R 2 taken together with the adjacent nitrogen atom represent a nitrogen-contain
α,α-Diphenylsuccinimide: Evaluation of anticonvulsant and hydrophobic properties
Jones,Amato,Jones
, p. 310 - 313 (2007/10/02)
The anticonvulsant potencies (ED50) of α,α-diphenylsuccinimide, phenytoin, and phenobarbital were evaluated in mice by a standard maximal electroshock technique. Potencies were expressed in terms of intraperitoneal dosage and blood and brain co