Comment on paper entitled: “Silica Sulfate as a recyclable and efficient catalyst for Beckmann rearrangement under microwave irradiation” [Journal of Molecular Catalysis A: Chemical 250 (2006) 100–103]

2006 ◽  
Vol 256 (1-2) ◽  
pp. 346-347 ◽  
Author(s):  
Mohammad Ali Zolfigol ◽  
Peyman Salehi
2020 ◽  
Vol 55 (2) ◽  
pp. 159-164
Author(s):  
WT Purba ◽  
PS Roy ◽  
S Jannat ◽  
SA Begum ◽  
MM Rahman

Rapid and efficient method for the synthesis of substituted olefins such as 2-(4-chlorophenylmethylene) malononitrile, 2-(4-hydroxyphenylmethylene) malononitrile and 2-cyano-3-(4-hydroxyphenyl) acrylamide etc under the influence of microwave irradiation are described. Urea has been utilized as an efficient catalyst for the Knoevenagel condensation of aldehydes with acidic active methylene compounds such as malononitrile, ethylcyanoacetate and cyanoacetamide to afford substituted olefins under the influence of microwave irradiation. The reaction proceeds smoothly under mild and solvent free conditions and the products are obtained in good yield. The method is applicable for a wide range of aldehydes including aromatic and heterocyclic substrates. Bangladesh J. Sci. Ind. Res.55(2), 159-164, 2020


2007 ◽  
Vol 2007 (10) ◽  
pp. 587-589 ◽  
Author(s):  
Mohan Babu Maradolla ◽  
Amaravathi Mandha ◽  
Chandra Mouli Garimella

Copper dipyridine dichloride (CuPy2Cl2) has been found to be an efficient catalyst for the synthesis of N-arylanthranilic acids from ortho halobenzoic acids and aromatic amines under microwave irradiation. Some of the advantages of this method are high chemoselectivity, ease of operation, less reaction times and high yields. (61–98%).


2005 ◽  
Vol 46 (50) ◽  
pp. 8691-8693 ◽  
Author(s):  
B. Rajitha ◽  
B. Sunil Kumar ◽  
Y. Thirupathi Reddy ◽  
P. Narsimha Reddy ◽  
N. Sreenivasulu

2010 ◽  
Vol 75 (10) ◽  
pp. 1315-1324 ◽  
Author(s):  
Abdolkarim Zare ◽  
Alireza Hasaninejad ◽  
Abolfath Parhami ◽  
Ahmad Moosavi-Zare ◽  
Fatemeh Khedri ◽  
...  

Quinoxaline derivatives were produced in excellent yields and short reaction times via the condensation of 1,2-diamines with 1,2-diketones in the neutral ionic liquid 1-butyl-3-methylimidazolium bromide ([bmim]Br) under catalyst-free and microwave irradiation conditions.


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