Fulvic Acid: An Efficient and Green Catalyst for the One-pot Four-component Domino Synthesis of Benzo[a]phenazine Annulated Heterocycles in Aqueous Medium

2020 ◽  
Vol 52 (1) ◽  
pp. 48-55 ◽  
Author(s):  
Afshin Yazdani-Elah-Abadi ◽  
Maliheh Razeghi ◽  
Nasim Shams ◽  
Mehrnoush Kangani ◽  
Razieh Mohebat
RSC Advances ◽  
2020 ◽  
Vol 10 (66) ◽  
pp. 40508-40513
Author(s):  
Sahar Saadat Hosseinikhah ◽  
Bi Bi Fatemeh Mirjalili ◽  
Naeimeh Salehi ◽  
Abdolahamid Bamoniri

Gum arabic-OPO3H2 (GA-OPO3H2) as a unique natural-based green catalyst was synthesized by the reaction of phosphorus pentoxide with gum arabic.


2016 ◽  
Vol 24 (2) ◽  
pp. 112-121 ◽  
Author(s):  
Mojtaba Lashkari ◽  
Malek Taher Maghsoodlou ◽  
Mahsa Karima ◽  
Belgais Adrom ◽  
Maryam Fatahpour

Abstract A straightforward, one-pot multicomponent synthesis of 1-(benzothiazolylamino)methyl-2-naphthol derivatives was achieved by condensation of 2-naphthol, aldehydes, and 2- aminobenzothiazole catalyzed by a small amount of citric acid, which acts as a benign enviermentally catalyst. Mild conditions with excellent yields and a simple isolation procedure are noteworthy advantages of this method.


2017 ◽  
Vol 41 (11) ◽  
pp. 673-675 ◽  
Author(s):  
Fahimeh Khazaee Feizabad ◽  
Khatereh Khandan-Barani ◽  
Alireza Hassanabadi

A high-yielding synthesis of 1,2,4,5-tetrasubstituted imidazoles is described, involving the reaction of 1,2-dicarbonyl compounds, aryl aldehydes, amines and ammonium acetate in the presence of a catalytic amount of glutamic acid under thermal, solvent-free conditions. The salient features of this protocol are aerobic conditions, a non-hazardous green catalyst, short reaction times and mild reaction conditions.


Synlett ◽  
2019 ◽  
Vol 30 (19) ◽  
pp. 2136-2142 ◽  
Author(s):  
Dariush Khalili ◽  
Leila Kavoosi ◽  
Ali Khalafi-Nezhad

An expeditious protocol for the one-pot synthesis of 1,4-disubstituted (β-hydroxy)-1,2,3-triazoles in an aqueous medium has been developed using copper aluminate nanoparticles. This heterogeneous catalytic system was found to drive a multicomponent click reaction between organic azides (generated in situ from epoxides or halides) and terminal aliphatic or aromatic alkynes in up to 96% yield without the need for a reducing agent. Structurally diverse 1,2,3-triazoles were synthesized in good to excellent yields, and the catalyst could be easily separated by simple filtration, recycled, and reused in six subsequent cycles.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Janardhan Banothu ◽  
Rajitha Bavantula ◽  
Peter A. Crooks

Highly efficient, ecofriendly, and improved protocol for the synthesis of 1,8-acridinediones has been developedviaone-pot multicomponent condensation of 1,3-cyclohexanedione/dimedone, aromatic aldehydes, and ammonium acetate utilizing poly(4-vinylpyridinium)hydrogen sulfate as catalyst in aqueous medium. Excellent yields in shorter reaction time, simple work-up procedure, easy recovery, and reusability of the catalyst are attractive features of this green protocol.


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