scholarly journals Microwave Assisted Solvent Free Synthesis of Azomethines from Aryl Aldehydes on Melamin Formaldehyde as Solid Support

2011 ◽  
Vol 8 (3) ◽  
pp. 1142-1145 ◽  
Author(s):  
Ramin Rezaei ◽  
Mohammad K. Mohammadi ◽  
Tahereh Ranjbar

Various aryl aldehydes underwent prompt one pot conversion into the corresponding azomethines in high yields by reacting with hydroxylamine hydrochloride supported on melamine formaldehyde under microwave irradiation.

2018 ◽  
Vol 42 (12) ◽  
pp. 604-607
Author(s):  
Loghman Firoozpour ◽  
Hoda Yahyavi ◽  
Ramona Ejtemaei ◽  
Setareh Moghimi ◽  
Alireza Foroumadi

A green and efficient method for preparing novel heterocyclic systems is established through the reaction of differently substituted benzaldehydes, barbituric acid and 4-amino-2H-chromene-2-one under solvent-free conditions. This method affords 6H-chromeno[3’,4’:5,6] pyrido[2,3-d]pyrimidine-trione derivatives in high yields and short reaction times.


1970 ◽  
Vol 24 ◽  
pp. 49-52 ◽  
Author(s):  
A D Mishra

A solid supported synthetic procedure has been developed for the synthesis of novel spiro indole derivatives using solid support as energy transfer medium under microwave irradiation (MWI). The results were compared with those obtained by the classical as well as solution phase method in MWI. This solvent-free technique coupled with the high yields and short reaction time makes this procedure eco-friendly for synthesis.  Keywords: Spiro indoles; Microwave irradiation; 1HNMR; IRDOI: 10.3126/jncs.v24i0.2391 Journal of Nepal Chemical Society Vol. 24, 2009 Page: 49-52  


2016 ◽  
Vol 147 (9) ◽  
pp. 1605-1614 ◽  
Author(s):  
Dawei Zhang ◽  
Xiaodong Chen ◽  
Xue Guo ◽  
Yumin Zhang ◽  
Yaya Hou ◽  
...  

2006 ◽  
Vol 3 (3) ◽  
pp. 164-168
Author(s):  
Li-Jun Li ◽  
Ying-Xia Song ◽  
Yan-Su Gao ◽  
Yan-Feng Li ◽  
Jian-Feng Zhang

Multistep and one-pot conversion of aldehydes to nitriles were carried out conveniently with out solvent using KF/Al2O3, montmorillonite KSF and K10 as catalyst, under microwave irradiation. The reactions are completed within 6-8 min to give satisfactory yields. KF/Al2O3was more effective catalyst both in multistep procedure and one-pot reaction.


RSC Advances ◽  
2014 ◽  
Vol 4 (46) ◽  
pp. 24001-24006 ◽  
Author(s):  
Kommuri Shekarrao ◽  
Partha Pratim Kaishap ◽  
Venkateshwarlu Saddanapu ◽  
Anthony Addlagatta ◽  
Sanjib Gogoi ◽  
...  

An efficient method was developed for the synthesis of pyrazole fused heterocycles via the palladium-catalyzed solvent free reaction of β-halovinyl/aryl aldehydes and 3-aminopyrazoles/5-aminopyrazoles under microwave irradiation in good yields.


2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Firouzeh Nemati ◽  
Azam Beyzai

A novel one-pot synthesis of 1,2-dihydro-1-arylnaphtho[1,2-e][1,3]oxazine-3-ones by condensation of a variety of aldehydes withβ-naphthol and urea or thiourea in the presence of wet cyanuric chloride under solvent-free condition has been described. High yields, simple procedure, easy workup, short reaction times, and avoiding the use of organic solvent are the advantages of this green methodology.


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