259747-30-3Relevant academic research and scientific papers
Cross-dehydrogenative regioselective Csp3-Csp2 coupling of enamino-ketones followed by rearrangement: An amazing formation route to acridine-1,8-dione derivatives
Sarkar, Rajib,Mukhopadhyay, Chhanda
, p. 2706 - 2715 (2016/03/05)
A new general method for the synthesis of acridine-1,8-diones through CDC coupling of enamino-ketones followed by rearrangement has been developed. This is a Cu(i) catalyzed procedure, based on the cross dehydrogenative coupling of the Csp3-H b
Efficient one-pot synthesis of acridinediones by indium(III) triflate-catalyzed reactions of β-enaminones, aldehydes, and cyclic 1,3-dicarbonyls
To, Quang Huy,Lee, Yong Rok,Kim, Sung Hong
, p. 1170 - 1176 (2012/07/14)
An efficient one-pot synthesis of acridinediones by In(OTf) 3-catalyzed reactions was developed starting from β-enaminones, aldehydes, and cyclic 1,3-diketones. The key strategies of these reactions involve domino Knoevenagel condensation/Michael addition/cyclodehydration reaction.
Ceric ammonium nitrate (CAN) catalyzed synthesis of N-substituted decahydroacridine-1,8-diones in PEG
Kidwai, Mazaahir,Bhatnagar, Divya
experimental part, p. 2700 - 2703 (2010/07/06)
Polyethylene glycol (PEG) was found to be an inexpensive non-toxic and effective medium for the one-pot synthesis of N-substituted decahydroacridine-1,8-diones in the presence of ceric ammonium nitrate (CAN) as the catalyst in high yields. Also, the solve
Proline-catalyzed simple and efficient synthesis of 1,8-dioxo- decahydroacridines in aqueous ethanol medium
Venkatesan,Pujari, Suresh S.,Srinivasan, Kumar V.
experimental part, p. 228 - 241 (2009/04/07)
Proline-catalyzed synthesis of 1,8-dioxo-decahydroacridines is achieved via one-pot, three-component condensation of aromatic aldehydes, cyclic diketone, and aryl amines in aqueous ethanol medium. This method offers the advantages of proceeding in neutral
