117358-62-0Relevant academic research and scientific papers
An efficient one-pot synthesis of polyhydrobenzoacridine-1-one derivatives under microwave irradiation without catalyst
Tu, Shujiang,Jia, Runhong,Jiang, Bo,Zhang, Yan,Zhang, Junyong
, p. 1621 - 1627 (2006)
A series of 3,3-dimethyl-9-substituted-1,2,3,4,9,10-hexahydrobenzo[c] acridine-1-ones and 3,3-dimethyl-9-substituted-1,2,3,4,9,10-hexahydrobenzo[a] acridine-1-ones were synthesized by the reaction of an aldehyde, α-naphthylamine or β-naphthylamine and dim
TiO2 nanoparticles as an efficient catalyst for the one-pot preparation of Tetrahydrobenzo[c]acridines in aqueous media
Abdolmohammadi, Shahrzad,Mohammadnejad, Mahdieh,Shafaei, Faezeh
, p. 362 - 366 (2013/06/26)
A series of tetrahydrobenzo[c]acridinone derivatives have been prepared by a one-pot fourcomponent reaction of 1-naphthol, aromatic aldehydes, dimedone, and ammonium acetate in aqueous media using a catalytic amount of titanium dioxide nanoparticles (TiO2 NPs). The advantages of this novel protocol include the excellent yields, operational simplicity, short reaction time, easy work-up, reusability of the catalyst and an environmentally friendly procedure.
A simple and clean procedure for the synthesis of polyhydroacridine and quinoline derivatives: Reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium
Wang, Xiang-Shan,Zhang, Mei-Mei,Zeng, Zhao-Sen,Shi, Da-Qing,Tu, Shu-Jiang,Wei, Xian-Yong,Zong, Zhi-Min
, p. 7169 - 7173 (2007/10/03)
A clean and simple synthesis of benzo[c]acridine, benzo[a]acridine, pyrido[2,3-c]acridine and benzo[f]quinoline derivatives was accomplished in good to excellent yields via the reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium catalyzed by TEBA. The structures were characterized by 1H NMR, IR and elemental analysis, and confirmed by X-ray diffraction study.
Synthesis and Spectra of 7-(o- and p-R-Phenyl)-10,10-dimethyl-8,9,10,11-tetrahydrobenzacridin-8-ones. Structure Correction of 1,2,3,4-Tetrahydro-2,2-dimethyl-5-aryl-6-aza-7,8-benzophenanthren-4-ones
Cortes, Eduardo,Martinez, Roberto,Avila, J. Gustavo,Toscano, R. Alfredo
, p. 895 - 899 (2007/10/02)
It has been reported that dimedone added to α-arylidennaphthylamines in ethanol with formation of 1,4-addition products derivatives of 5-aryl-5,6,7,8,9,10-hexahydrobenzophenanthridin-7-ones, III, which are easily oxidized by chromic anhydride to the co
