72916-49-5Relevant academic research and scientific papers
Synthesis, molecular modeling study, preliminary antibacterial, and antitumor evaluation of N-substituted naphthalimides and their structural analogues
El-Azab, Adel S.,Alanazi, Amer M.,Abdel-Aziz, Naglaa I.,Al-Suwaidan, Ibrahim A.,El-Sayed, Magda A. A.,El-Sherbeny, Magda A.,Abdel-Aziz, Alaa A.-M.
, p. 2360 - 2375 (2013/07/26)
Carboxylic acid imides 1-26 have been synthesized and screened for their antibacterial against gram-positive and gram-negative organisms and their antitumor activity against 60 tumor cell lines taken from nine different organs. Compounds 12, 14, and 16 we
Copper-promoted N-arylations of cyclic imides within six-membered rings: A facile route to arylene-based organic materials
Chernick, Erin T.,Ahrens, Michael J.,Scheidt, Karl A.,Wasielewski, Michael R.
, p. 1486 - 1489 (2007/10/03)
(Chemical Equation Presented) Cyclic imides within six-membered rings are shown to undergo efficient N-arylation using various arylboronic esters mediated by copper(II) acetate in the presence of an amine base and oxygen atmosphere with gentle heating. Until now, the synthesis of N-arylated cyclic imides having six-membered rings was restricted largely to strongly heating anilines in the presence of anhydrides. This reaction is applicable to the synthesis of new organic materials based on arylene imide and bis(imide) dyes, such as perylene-3,4: 9,10-bis(dicarboximide)s.
N-SUBSTITUTED ISONAPHTHALIMIDES. FORMATION AND REACTION WITH AMINES
Ganin, E. V.,Makarov, V. F.,Nikitin, V. I.
, p. 2209 - 2215 (2007/10/02)
N-Substituted isonaphthalimides and N-substituted naphthalimides, as considered previously, are formed in the reaction of 1,8-naphthaloyl chloride with primary amines.The reaction of N-substituted isonaphthalimides with sterically unhindered amines leads to the N,N'-substituted diamides of 1,8-naphthalenedicarboxylic acid.In the case of sterically hindered amines it results in isomerization to the N-substituted naphthalimides.The thermolysis of the N,N'-substituted diamides of 1,8-naphthalenedicarboxylic acid leads to amines and N-substituted naphthalimides.
