Chemical fixation of CO 2: efficient synthesis of quinazoline-2, 4 (1H, 3H)-diones catalyzed by guanidines under solvent-free conditions
J Gao, LN He, CX Miao, S Chanfreau
Index: Gao, Jian; He, Liang-Nian; Miao, Cheng-Xia; Chanfreau, Sebastien Tetrahedron, 2010 , vol. 66, # 23 p. 4063 - 4067
Full Text: HTML
Citation Number: 57
Abstract
Guanidines were proved to be efficient catalysts for the chemical fixation of carbon dioxide with 2-aminobenzonitriles under solvent-free conditions. Notably, the catalysts with low loading worked well for a variety of 2-aminobenzonitriles. As a result, quinazoline-2, 4 (1H, 3H)-diones by employing present protocol were obtained in good yields under mild conditions. This process represents an alternative approach for the greener chemical ...
Related Articles:
Superbase-derived protic ionic liquids with chelating fluorinated anions
[Bell, Jason R.; Luo, Huimin; Dai, Sheng Tetrahedron Letters, 2011 , vol. 52, # 29 p. 3723 - 3725]
[Li, Shenghai; Lin, Yingjie; Cao, Jungang; Zhang, Suobo Journal of Organic Chemistry, 2007 , vol. 72, # 11 p. 4067 - 4072]
Superbase-derived protic ionic liquids with chelating fluorinated anions
[Bell, Jason R.; Luo, Huimin; Dai, Sheng Tetrahedron Letters, 2011 , vol. 52, # 29 p. 3723 - 3725]