1046467-94-0Relevant articles and documents
Tris(pentafluorophenyl)borane-catalyzed three-component reaction for the synthesis of 1,8-dioxodecahydroacridines under solvent-free conditions
Chandrasekhar, Srivari,Rao, Yaragorla Srinivasa,Sreelakshmi, Leila,Mahipal, Bodugam,Reddy, Chada Raji
, p. 1737 - 1740 (2008)
A mild and efficient method for the synthesis of 1,8- dioxodecahydroacridines has been developed. The synthesis proceeds via a three-component reaction of a 1,3-dione, an aldehyde and an amine, under solvent-free conditions, catalyzed by tris(pentafluorophenyl)borane [B(C 6F5)3]. The mildness of the catalyst was demonstrated by studying the reaction of 1,3-cyclohexanedione with various aldehydes and amines which gave the 1,8-dioxo-decahydroacridines in high yields.
Efficient iron catalyzed ligand-free access to acridines and acridinium ions
Bhuyan, Samuzal,Chhetri, Karan,Mandal, Susanta,Roy, Biswajit G.
supporting information, p. 3178 - 3185 (2020/06/18)
Acridines and acridinium ions are one of the important classes of compounds in terms of their usefulness in pharmaceuticals, materials, dyes and photo-catalysis. Here we present an unconventional FeCl3-alcohol catalysed one-pot method for their
