ChemInform Abstract: Reactions of 6-Aminouracils - A Novel and Highly Efficient Procedure for Preparation of Some New Spiro Pyridodipyrimidines under Classical or Microwave-Assisted Solvent-Free Conditions.

ChemInform ◽  
2009 ◽  
Vol 40 (7) ◽  
Author(s):  
Mohammad R. Mohammadizadeh ◽  
Javad Azizian ◽  
Fatemeh Teimouri ◽  
Ali A. Mohammadi ◽  
Ali R. Karimi ◽  
...  
2008 ◽  
Vol 86 (9) ◽  
pp. 925-929 ◽  
Author(s):  
Mohammad R Mohammadizadeh ◽  
Javad Azizian ◽  
Fatemeh Teimouri ◽  
Ali A Mohammadi ◽  
Ali R Karimi ◽  
...  

A versatile and highly efficient procedure has been introduced for preparation of spiro pyridodipyrimidines during the investigation of the reaction of 1,3-dimethyl-6- aminouracil with isatin derivatives, ninhydrin, and acenaphthoquinone under classical or microwave-assisted solvent-free conditions.Key words: isatin, ninhydrin, acenaphtoquinone, 1,3-dimethyl-6-aminouracil, solvent-free.


2008 ◽  
Vol 86 (4) ◽  
pp. 317-324 ◽  
Author(s):  
Abdolkarim Zare ◽  
Alireza Hasaninejad ◽  
Mohammad Hassan Beyzavi ◽  
Abolfath Parhami ◽  
Ahmad Reza Moosavi Zare ◽  
...  

An efficient procedure for the synthesis of carboacyclic nucleosides via microwave-assisted Michael addition of pyrimidine and purine nucleobases to α,β-unsaturated esters in the presence of catalytic amounts of zinc oxide (ZnO) and tetrabutylammonium bromide (TBAB) is described. The reactions proceed rapidly in good to excellent yields.Key words: ZnO–TBAB, green chemistry, Michael addition, nucleobase, solvent-free, microwave.


2009 ◽  
Vol 52 (12) ◽  
pp. 2166-2170 ◽  
Author(s):  
XueZheng Liang ◽  
Lu Chen ◽  
HaiHong Wu ◽  
JianGuo Yang ◽  
MingYuan He

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