Supramolecular β-cyclodextrin as a Biodegradable and Reusable Catalyst Promoted Environmentally Friendly Synthesis of Pyrano[2,3-d]pyrimidine Scaffolds via Tandem Knoevenagel–Michael–Cyclocondensation Reaction in Aqueous Media

Author(s):  
Farzaneh Mohamadpour
RSC Advances ◽  
2016 ◽  
Vol 6 (60) ◽  
pp. 55319-55326 ◽  
Author(s):  
Reza Tayebee ◽  
Kokab Savoji ◽  
Maryam Kargar Razi ◽  
Behrooz Maleki

An efficient protocol for the synthesis of C3-symmetrical 1,3,5-triarylbenzenes under solvent-free conditions. γ-Al2O3/H5PW10V2O40 nanocomposite is introduced as a highly reusable catalyst.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Pradeep Paliwal ◽  
Srinivasa Rao Jetti ◽  
Anjna Bhatewara ◽  
Tanuja Kadre ◽  
Shubha Jain

The reaction of 5,5-dimethylcyclohexane-1,3-dione with various heteroarylaldehydes afforded the corresponding heteroaryl substituted xanthene derivatives 1(a–f). The reaction proceeds via the initial Knoevenagel, subsequent Michael, and final heterocyclization reactions using 1,4-diazabicyclo[2.2.2]octane (DABCO) as a catalyst in aqueous media. The synthesized heteroaryl substituted xanthenes 1(a–f) reacted with malononitrile to obtain different alkylidenes 2(a–f). Short reaction time, environmentally friendly procedure, avoiding of cumbersome apparatus, and excellent yields are the main advantages of this procedure which makes it more economic than the other conventional methods.


ChemInform ◽  
2007 ◽  
Vol 38 (45) ◽  
Author(s):  
K. Rajender Reddy ◽  
C. V. Rajasekhar ◽  
G. Gopi Krishna

Author(s):  
Pham Xuan Thao

Thioamides have been widely used in the fields of medicine and organic chemistry, some of which are essential bioactive compounds, plant protection agents, and drugs. It could also be used as a vulcanizing agent, an additive to lubricants and greases, and a ligand in organic synthesis. Usually, thioamide is synthesized at high temperatures or in the microwave using an expensive noble metal complex as catalysts. This paper presented a straightforward method for synthesizing thioamides by using N-tert-butylsulfinyl amide, aldehyde, and sulfur. The reaction was carried out in water, which is an environmentally friendly solvent. The reaction selectivity and yield were up to 89%.


2018 ◽  
Vol 42 (12) ◽  
pp. 614-617
Author(s):  
Soumia Belkharchach ◽  
Hanane Elayadi ◽  
Hana Ighachane ◽  
Said Sebti ◽  
Mustapha Ait Ali ◽  
...  

2-Substituted benzimidazoles are selectively synthesised in high yields via the condensation of o-phenylenediamine derivatives with aldehyde derivatives using catalytic amount of p-toluenesulfonic acid coated natural phosphate (NP/PTSA) under mild conditions. The use of NP/PTSA as a reusable catalyst makes this process simple, convenient, and environmentally friendly.


2012 ◽  
Vol 5 (2) ◽  
pp. 139-145 ◽  
Author(s):  
Vikas S. Padalkar ◽  
Vinod D. Gupta ◽  
Kiran R. Phatangare ◽  
Vikas S. Patil ◽  
Prashant G. Umape ◽  
...  

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