363569-99-7Relevant academic research and scientific papers
Choline chloride catalyzed eco-friend and effective one-pot synthesis of 9-arylacridine-1,8-dione and hexahydroquinoline via Hantzsch type reaction
Mao, Shengxue,Li, Fei,Lv, Yue,Lv, Chengwei,Yu, Shijun
, p. 1895 - 1902 (2017)
Choline chloride was utilized to efficiently catalyzed Hantzsch type reaction for the synthesis of 9-arylacridine-1,8-dione and hexahydroquinoline derivatives. The optimized catalytic system benefits from facile operation and separation procedures, in goo
An Efficient One-Pot Four-Component Synthesis of 9-Aryl-Hexahydroacridine-1,8-Dione Derivatives in the Presence of a Molecular Sieves Supported Iron Catalyst
Magyar, ágnes,Hell, Zoltán
, p. 2528 - 2534 (2019/06/19)
Abstract: A series of 9-aryl-hexahydroacridine-1,8-diones are synthetized with good to excellent yields (50–99%) via a one-pot four-component reaction of dimedone, aromatic aldehydes and ammonium acetate in the presence of 4?? molecular sieves modified wi
N-Propyl benzoguanamine sulfonic acid supported on magnetic Fe3O4 nanoparticles: A novel and efficient magnetically heterogeneous catalyst for the synthesis of 1,8-dioxo-decahydroacridine derivatives
Gholami Dehbalaei, Masoumeh,Foroughifar, Naser,Pasdar, Hoda,Khajeh-Amiri, Alireza
supporting information, p. 327 - 335 (2017/12/28)
In this study, N-propyl-benzoguanamine-SO3H-stabilized magnetic nanoparticles were prepared as a new heterogeneous acid catalyst in accordance with the principles of green chemistry. The new catalyst is used for the synthesis of derivatives of
Efficient synthesis of acridinediones in aqueous media
Tiwari, Keshri Nath,Uttam, Mane Rajendra,Kumari, Puja,Vatsa, Piyush,Prabhakaran
, p. 1013 - 1019 (2017/05/04)
An efficient synthesis of acridinediones in two steps have been achieved using water as a reaction media without chromatographic purification. First step involves the reaction of dimedone with ammonium acetate to yield enaminone in water which on further
Green and efficient synthesis of acridine-1,8-diones and hexahydroquinolines via a KH2PO4 catalyzed Hantzsch-type reaction in aqueous ethanol
Yü, Shi-Jun,Wu, Si,Zhao, Xin-Min,Lü, Cheng-Wei
, p. 3121 - 3130 (2017/04/19)
Abstract: A simple, clean, and economical methodology for the synthesis of acridine-1,8-dione and hexahydroquinoline derivatives via Hantzsch-type condensation has been described. This study highlights the development of a new green pathway for the prepar
Solvent-free synthesis of polyhydroquinoline and 1,8-dioxodecahydroacridine derivatives through the Hantzsch reaction catalyzed by a natural organic acid: A green method
Sehout, Imène,Boulcina, Raouf,Boumoud, Boudjemaa,Boumoud, Taous,Debache, Abdelmadjid
supporting information, p. 1185 - 1191 (2017/06/09)
Solvent-free and high yielding one-pot synthesis of 1,8-dioxodecahydroacridine and polyhydroquinoline derivatives have been described through Hantzsch condensation of various aldehydes, ammonium acetate with cyclic 1,3-dicarbonyl compounds and ethyl aceto
Solvent-free synthesis of dihydropyridines and acridinediones via a salicylic acid-catalyzed hantzsch multicomponent reaction
Khodja, Imene Amine,Ghalem, Wassima,Dehimat, Zineb Imene,Boulcina, Raouf,Carboni, Bertrand,Debache, Abdelmadjid
supporting information, p. 959 - 967 (2014/03/21)
A multicomponent Hantzsch synthesis of 1,4-dihydropyridines and acridinediones from commercially available aldehydes, ammonium acetate, and ethyl acetoacetate or dimedone, in the presence of salicylic acid as an efficient catalyst, in good yield and short reaction time is reported. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]
