713095-56-8Relevant articles and documents
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 (2007/10/03)
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
A clean synthesis of polyhydroacridine and indenoquinoline derivatives catalyzed by triethylbenzylammonium chloride in aqueous media
Wang, Xiang-Shan,Zhang, Mei-Mei,Zeng, Zhao-Sen,Shi, Da-Qing,Tu, Shu-Jiang,Wei, Xian-Yong,Zong, Zhi-Min
, p. 989 - 995 (2007/10/03)
An efficient and convenient synthesis of benzo[a]acridines and indeno[1,2-b]benzo[f]quinolines was achieved in high yields by the reaction of N-arylidenenaphthalen-2-amine with 1,3-dicarbonyl compounds catalyzed with triethylbenzylammmonium chloride (TEBA
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.
