A Facile Three-Component One-Pot Synthesis of Some Novel Tricyclic Hetero-Ring Systems

2015 ◽  
Vol 53 (6) ◽  
pp. 1892-1896 ◽  
Author(s):  
Sobhi M. Gomha ◽  
Fathy M. Abdelrazek
ChemInform ◽  
2010 ◽  
Vol 28 (29) ◽  
pp. no-no
Author(s):  
C. KAEPPLINGER ◽  
R. BECKERT ◽  
W. GUENTHER ◽  
H. GOERLS

1994 ◽  
Vol 35 (49) ◽  
pp. 9293-9296 ◽  
Author(s):  
Achille Barco ◽  
Simonetta Benetti ◽  
Carmela De Risi ◽  
Gian P. Pollini ◽  
Romeo Romagnoli ◽  
...  

2021 ◽  
pp. 56-63
Author(s):  
Muna A. Othman Salem ◽  
Hana A. A. Mageed ◽  
Huda S. Muftah ◽  
Reda F. El- Ezabi ◽  
Fayrouz A. Khaled

An efficient and facile one pot synthesis of 3,4-dihydropyrimidinones (Belinelli compound) from furfural, acetylacetone and urea under solvent free conditions was performed, resulted in promising yield. These compounds reacted with benzaldehyde and furfural to give the corresponding chalcones. Chalcones are used to synthesize several derivatives like pyrazolines isoxazoles and pyrimidines having different heterocyclic ring systems. Keywords: Belinelli compounds; Chalcone; Pyrazolines isoxazoles; Pyrimidines


ChemInform ◽  
2010 ◽  
Vol 26 (18) ◽  
pp. no-no
Author(s):  
A. BARCO ◽  
S. BENETTI ◽  
C. DE RISI ◽  
G. P. POLLINI ◽  
R. ROMAGNOLI ◽  
...  

2017 ◽  
Vol 4 (3) ◽  
pp. 431-444 ◽  
Author(s):  
Pei-Qiang Huang ◽  
Ying-Hong Huang ◽  
Shu-Ren Wang

We report a versatile approach for the one-pot synthesis of substituted pyrrolidine, piperidine, indolizidine, and quinolizidine ring systems, and enimino carbocycles.


1997 ◽  
Vol 1997 (3) ◽  
pp. 617-622 ◽  
Author(s):  
Christian Käpplinger ◽  
Rainer Beckert ◽  
Wolfgang Günther ◽  
Helmar Görls

2019 ◽  
Vol 97 (9) ◽  
pp. 690-696 ◽  
Author(s):  
Kambappa Vinaya ◽  
Ganganahalli K. Chandrashekara ◽  
Prasanna D. Shivaramu

1,2,4-Oxadiazole is one of the most promising heterocyclic ring systems in medicinal chemistry. In the present paper, we report the method for an efficient one-pot synthesis of 3,5-diaryl substituted 1,2,4-oxadiazoles using a two-component reaction of gem-dibromomethylarenes with amidoximes in good yields. In this method, gem-dibromomethylarenes are used as benzoic acid equivalents for the efficient synthesis of aryl-substituted 1,2,4-oxadiazoles. It is anticipated that this methodology will have versatile applications in the practical syntheses of various molecules of both medicinal and material chemistry importance.


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