137093-53-9Relevant academic research and scientific papers
Aliphatic C-H/π and heteroatom/π interactions in N-aryl-3,4- (9′,10′-dihydroanthracene-9′,10′-diyl)succinimides
Raimondi, Laura,Benaglia, Maurizio,Cozzi, Franco
, p. 4993 - 4998 (2014/08/18)
A series of N-aryl-3,4-(9′,10′-dihydroanthracene-9′, 10′-diyl)succinimides have been synthesized as model compounds to study the interaction of an aromatic π system with aliphatic H atoms and heteroatoms such as oxygen, sulfur, and fluorine. The steric re
Structural studies of N-(2′-substituted phenyl)-9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboximides by X-ray diffraction and NMR spectroscopy - Proofs for CH/π interactions in liquid and solid phases
Grossmann, Gisbert,Potrzebowski, Marek J.,Olejniczak, Sebastian,Ziolkowska, Natasza E.,Bujacz, Grzegorz D.,Ciesielski, Wlodzimierz,Prezdo, Wiktor,Nazarov, Valerii,Golovko, Vladislav
, p. 1095 - 1101 (2007/10/03)
N-(2′-R-Phenyl)-9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboximides with R = Me (1), OMe (2), OEt (3) and H (4) were investigated. The crystal and molecular structures of 1-3, determined by single crystal methods, show different conformations of the N
Torsional barriers about N-C (aryl) bond and atropisomerism: A 1H NMR study
Srivastav, Kamal K.,Verma, Ashok K.,Verma, Shiva M.
, p. 1143 - 1148 (2007/10/02)
Role of substituents at 3',4',5' and 6'-positions in N-arylsuccinimidyl system on the torsional barrier about aryl-N bond has been reported with the help of asymmetric cage moiety through VT NMR studies of o-methyl resonances.Substituents at 3'-position r
Modular Design of Hosts Involving a Rigid Succinimide Framework and N-Bonded Lateral Groups. Crystalline Inclusion Properties and Crystal Structures of Inclusion Compounds with Dioxane, MeOH, and DMF
Weber, Edwin,Finge, Stephan,Csoeregh, Ingeborg
, p. 7281 - 7288 (2007/10/02)
A series of crystalline host molecules comprising a characteristic 9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboxamide framework have been synthesized and studied with regard to their inclusion behavior.They follow a new design concept which is to conv
Stereochemical Investigation by PMR Spectroscopy : Nucleophilic Addition to a Carbonyl Function in Sterically Hindered System
Singh, Narain,Verma, Shiva Mohan
, p. 873 - 877 (2007/10/02)
Stereochemistry of the nucleophilic addition to one of the carbonyls of the succinimidyl ring of α,β-(9,10-dihydroanthracene-9,10-diyl)-ortho substituted N-phenylimides (3) has been investigated by PMR spectroscopy.Addition has been found to be stereosele
