Waste mussel shell as a highly efficient heterogeneous catalyst for the synthesis of polyfunctionalized 4H-pyrans in aqueous media

被引:0
作者
U. P. Patil
Rupesh C. Patil
Suresh S. Patil
机构
[1] ACS College,Department of Chemistry
[2] Affiliated To Shivaji University,Green Chemistry Research Laboratory
[3] SMDBS College,Synthetic Research Laboratory, PG Department of Chemistry
[4] Affiliated to Shivaji University,undefined
[5] PDVP College,undefined
[6] Affiliated To Shivaji University,undefined
来源
Reaction Kinetics, Mechanisms and Catalysis | 2020年 / 129卷
关键词
Heterogeneous catalyst; Mussel shell; Green solvent; 4; -pyrans;
D O I
暂无
中图分类号
学科分类号
摘要
An economical and environmentally friendly heterogeneous base catalyst has been developed from a waste freshwater mussel shell and employed successfully for the synthesis of 4H-pyrans in an aqueous medium at ambient temperature. 2-arylidenemalononitrile, an intermediate of 4H-pyran reaction, was also prepared using the same catalyst. The catalyst was characterized by FT-IR, XRD, XRF, EDS, and SEM. Analytical tools such as XRF and EDS explored the presence of calcium oxide as a main component in the mussel shell, while the XRD pattern showed crystalline nature and SEM image displayed porous surface with irregular cavities. The catalyst exhibited unprecedented performance in the one-pot three-component condensation reaction of C–H activated acidic compounds with aromatic aldehydes and malononitrile in the green reaction medium and offered pure products without chromatographic separation.
引用
收藏
页码:679 / 691
页数:12
相关论文
共 167 条
[1]  
Flavin MT(1996)Synthesis, chromatographic resolution, and anti-human immunodeficiency virus activity of (+/-)-calanolide A and its enantiomers J Med Chem 39 1303-1313
[2]  
Rizzo JD(2005)Synthesis and anti-inflammatory activity of coumarin derivatives J Med Chem 48 6400-6408
[3]  
Khilevich A(2002)Synthesis of halogen derivatives of benzo[ Farmaco 57 715-722
[4]  
Kucherenko A(2010)]chromene and benzo[ Eur J Med Chem 45 790-794
[5]  
Sheinkmn AK(2006)]anthracene with promising antimicrobial activities Bioorg Med Chem 14 6686-6694
[6]  
Vilaychack V(2011)Cytotoxic activity of 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones and 4-oxo-4 Bioorg Med Chem 19 7357-7364
[7]  
Lin L(2008)-chromene-3-carbothionic acid J Med Chem 51 417-423
[8]  
Chen W(1996)-phenylamides Curr Med Chem 3 227-238
[9]  
Greenwood EM(1995)A novel QSAR model for predicting induction of apoptosis by 4-aryl-4 Curr Med Chem 2 573-582
[10]  
Pengsuparp T(2004)-chromenes Synlett 5 871-873