A Mild, Efficient and Environmentally Friendly Method for the Regio- and Chemoselective Synthesis of Enaminones Using Bi(TFA)3 as a Reusable Catalyst in Aqueous Media.

ChemInform ◽  
2004 ◽  
Vol 35 (23) ◽  
Author(s):  
Ahmad R. Khosropour ◽  
Mohammad M. Khodaei ◽  
Mehdi Kookhazadeh
2021 ◽  
Vol 37 (2) ◽  
pp. 341-347
Author(s):  
Arup Datta

In this work simple efficient, one pot and environmentally friendly method was developed for the synthesis of 2-Aryl-1H-benzoxazole derivatives at 80º C using ortho-aminophenol and various aldehydes. It has been found that Dowex50W is an effective catalyst to prepare moderate to high yield of a variety of benzoxazole derivatives through a clean and simple process. Aqueous medium, green methodology, rapid reaction, reusability of heterogeneous catalyst are the great advantages of this protocol.


2015 ◽  
Vol 3 (45) ◽  
pp. 11945-11952 ◽  
Author(s):  
Wei Lyu ◽  
Jiangtao Feng ◽  
Wei Yan ◽  
Charl FJ Faul

An environmentally friendly method is developed to explore the self-assembly of Ph/NH2-capped tetra(aniline) nanowires in acidic aqueous medium with ultrasonic irradiation.


RSC Advances ◽  
2015 ◽  
Vol 5 (45) ◽  
pp. 35425-35434 ◽  
Author(s):  
Ahmad Amiri ◽  
Rad Sadri ◽  
Goodarz Ahmadi ◽  
B. T. Chew ◽  
S. N. Kazi ◽  
...  

In order to improve the dispersibility of multi-walled carbon nanotubes (MWCNT) in aqueous media, MWCNT were functionalized with tetrahydrofurfuryl polyethylene glycol (TFPEG) in a one-pot, fast and environmentally friendly method.


2006 ◽  
Vol 2006 (5) ◽  
pp. 342-344 ◽  
Author(s):  
Hanakere R. Girisha ◽  
Gejjalagere R. Srinivasa ◽  
D. Channe Gowda

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.


2009 ◽  
Vol 140 (12) ◽  
pp. 1489-1494 ◽  
Author(s):  
Valiollah Mirkhani ◽  
Majid Moghadam ◽  
Shahram Tangestaninejad ◽  
Iraj Mohammadpoor-Baltork ◽  
Mohammad Mahdavi

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.


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