Synthesis of 1,8-Dioxo-decahydroacridine Derivatives <i>via</i> Ru-Catalyzed Acceptorless Dehydrogenative Multicomponent Reaction
作者:Nandita Biswas、Dipankar Srimani
DOI:10.1021/acs.joc.1c01075
日期:2021.7.16
A Ru-catalyzed acceptorless dehydrogenative multicomponent reaction has been developed. This reaction offers a cost-effective and simple operational strategy to synthesize biologically active 1,8-dioxodecahydroacridine derivatives. The protocol provides a wide range of substrate scope and various functional groups are also well tolerated under the reaction condition. To shed light on the mechanistic
A green procedure for the synthesis of 1,8-dioxodecahydroacridine derivatives under microwave irradiation in aqueous media without catalyst
作者:Zi-Qiang Tang、Yan Chen、Chang-Ning Liu、Ke-Ying Cai、Shu-Jiang Tu
DOI:10.1002/jhet.322
日期:——
A green procedure for the synthesis of 1,8‐dioxo‐decahydroacridine derivatives is developed undermicrowaveirradiationwithoutcatalyst in water. This method provides several advantages such as excellent yields (86–96%), simple workup procedure, and environment friendliness. J. Heterocyclic Chem., (2010).
Sulfuric acid-modified poly(vinylpyrrolidone) ((PVP–SO<sub>3</sub>H)HSO<sub>4</sub>): a new highly efficient, bio-degradable and reusable polymeric catalyst for the synthesis of acridinedione derivatives
Synthesis of 1,8-Dioxo-Decahydroacridines using Pyridinium Hydrogen Sulfate Ionic Liquid as an Green, Efficient and Reusable Catalyst
作者:Somaye Karimian、Hassan Tajik
DOI:10.2174/1570178613666160104232735
日期:2016.2.10
amine (1 mmol), PHSIL (0.65 mmol), CH3CN (3 mL) at 80°C, a series of 1,8-dioxo-decahydroacridines were synthesized via the one-pot three component reaction between various aromatic aldehydes and amines with dimedone. The aromatic aldehydes containing electrondonating and electron-withdrawing groups afforded 1,8-dioxo-9-aryl-10-aryl-decahydroacridines with high yields within short reaction times in
A novel cascade reaction of Schiff'sbase was described. The products afforded in the reaction depended on the ratio of the two starting materials. A possible mechanism of the reactions is proposed, which underwent the breaking and new formation of the bond between carbon atom and nitrogen atom.