A novel amino acid functionalized ionic liquid promoted one-pot solvent-free synthesis of 3,4-dihydropyrimidin-2-(1H)-thiones

2012 ◽  
Vol 39 (3) ◽  
pp. 1335-1342 ◽  
Author(s):  
Parasuraman Karthikeyan ◽  
Sythana Suresh Kumar ◽  
Aswar Sachin Arunrao ◽  
Muskawar Prashant Narayan ◽  
Pundlik Rambhau Bhagat
ChemInform ◽  
2010 ◽  
Vol 42 (1) ◽  
pp. no-no
Author(s):  
Abolghasem Davoodnia ◽  
Mehdi Bakavoli ◽  
Raheleh Moloudi ◽  
Niloofar Tavakoli-Hoseini ◽  
Maryam Khashi

2018 ◽  
Vol 42 (8) ◽  
pp. 428-433 ◽  
Author(s):  
Song Bai ◽  
Shan Liu ◽  
Yunying Zhu ◽  
Jiali Lu ◽  
Lina Ai ◽  
...  

An efficient asymmetric synthesis of chiral β-amino acid ester derivatives containing a 4-(pyridin-3-yl)pyrimidin-2-yl amine moiety was developed. This catalytic asymmetric Mannich reaction gave target products in high yields (95%) and excellent enantioselectivities (>99% ee) using a cinchona-based squaramide catalyst under solvent-free, one-pot conditions. Antiviral bioassays indicated that some of the chiral products exhibited higher antiviral activities against tobacco mosaic virus than the commercial compound ribavirin.


2016 ◽  
Vol 70 (8) ◽  
Author(s):  
Heshmatollah Alinezhad ◽  
Mahmood Tajbakhsh ◽  
Mahboobeh Zare ◽  
Mahbooeh Mousavi

AbstractA one-pot three-component Biginelli-like reaction of enaminones, aldehydes with urea/thiourea in the presence of 2-pyrrolidonium bisulphate as an acidic ionic liquid catalyst for the preparation of 6-unsubstituted dihydropyrimidinones is described. The excellent yield, short reaction time, simple procedure and avoidance of the use of organic solvents are some advantages of this method.


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