pyrimidinones and terephthalic-acid

pyrimidinones has been researched along with terephthalic-acid* in 1 studies

Other Studies

1 other study(ies) available for pyrimidinones and terephthalic-acid

Article	Year
Shaken not stirred: a facile synthesis of 1,4-bis(furo[2,3-d]-pyrimidine-2,4(1H,3H)-dione-5-yl)benzenes by one-pot reaction of isocyanides, N,N'-dimethylbarbituric acid, and terephthaldialdehyde. Bioorganic & medicinal chemistry letters, 2006, Jul-15, Volume: 16, Issue:14 A simple and efficient synthesis of 1,4-bis(furo[2,3-d]pyrimidine-2,4(1H,3H)-dione-5-yl)benzene derivatives was achieved via a one-pot three-component reaction of isocyanides, N,N'-dimethylbarbituric acid, and terephthaldialdehyde in DMF at room temperature for 30 min. These improved reaction conditions allow the preparation of highly substituted furopyrimidinones in high yields and purity under mild reaction conditions. Topics: Aldehydes; Barbiturates; Benzene Derivatives; Cyanides; Furans; Magnetic Resonance Spectroscopy; Models, Chemical; Phthalic Acids; Pyrimidinones; Spectrophotometry, Ultraviolet	2006

Article

Year

Shaken not stirred: a facile synthesis of 1,4-bis(furo[2,3-d]-pyrimidine-2,4(1H,3H)-dione-5-yl)benzenes by one-pot reaction of isocyanides, N,N'-dimethylbarbituric acid, and terephthaldialdehyde.

Bioorganic & medicinal chemistry letters, 2006, Jul-15, Volume: 16, Issue:14

A simple and efficient synthesis of 1,4-bis(furo[2,3-d]pyrimidine-2,4(1H,3H)-dione-5-yl)benzene derivatives was achieved via a one-pot three-component reaction of isocyanides, N,N'-dimethylbarbituric acid, and terephthaldialdehyde in DMF at room temperature for 30 min. These improved reaction conditions allow the preparation of highly substituted furopyrimidinones in high yields and purity under mild reaction conditions.

Topics: Aldehydes; Barbiturates; Benzene Derivatives; Cyanides; Furans; Magnetic Resonance Spectroscopy; Models, Chemical; Phthalic Acids; Pyrimidinones; Spectrophotometry, Ultraviolet

2006