Downloads provided by UsageCounts
{"references": ["1.\tIndalkar K.S, Manisha S. P, Chaturbhuj G. U, Tetrahedron Letters, 2017, 10, 1016. 2.\tKhurana J. M, Magoo, D, Tetrahedron Lett., 2009, 50, 7300. 3.\tElnagdi M. H, Elmoghayar M.R.H., Sadek, K. U., Adv. Heterocyclic Chem., 1990, 48, 223. 4.\tKuo, S. G, Huang J and Nakamura H., J. Med. Chem., 1984,27, 539. 5.\tWang J. L, Liu D., Zheng Z. J., Shan S, Hax X., Proc. Natl Acad. Sci. USA, 2009, 97, 7124-7129. 6.\tZaki M.E.A, Saliman H. A., Hickal O. A., Rashed A. E. Z, Z. Natureforsch C, 2006, 61, 1-5. 7.\tLiu Z, Zhang R, Meng Q, Zhang X, Sun Y, Med. Chem. Common, 2016, 7, 1352. 8.\tVasuki G, Kumaravel K, Tetrahedron Lett., 2008, 49, 5636. 9.\tLitvinov Y. M., Shestrpalov A. A, Rtinovskaya L. A., Shestopalov A. M., J. Comp. Chem., 2009, 11, 914. 10.\tMecadon H, Rohman M. R., Kharbanger I., Laloo B. K., Kharkonger I, Rajbanjshi M, Myrboh B., Tetahedron Lett., 2011, 52, 3228. 11.\tKarimi-Jaberi, Z Sham, M. M. R., Poolrdian B, Acta Chim Slon. 2013, 60, 105. 12.\tMadhusudana Reddy M. B., Pasha M. A., Indian, J. Chem., 2012, 51B, 537. 13.\tEbrahimi J, Mohammadi A, Pakjoo V, Bahrmzade E, Habibi A, J. Chemi. Sci., 2012, 124, 1013. 14.\tBihani M, Bora P. P., Bez G, Askari H., ACS Sustain. Chem. Eng., 2013, 1, 440. 15.\tBabaie M, Seibani H, Arb. J. Chem., 2014, 4, 159. 16.\tChavan H. V., Baba S. B., Hoval R. U., Bandgra B. P., Bull Korean Chem. Soc., 2011, 32, 3963. 17.\tWaghmare A. S., Pandit S. S., J. Saudi Chem. Soc., 2017, 21, 286. 18.\tRavi P and Tewari S. P, Catalysis Communications, 2012, 19, 37. 19.\tSuzuki H., Ikegami T., Matano Y, Synthesis, 1997, 249. 20.\tMarch J. Advanced Organic Chemistry, 4th Ed. John Wiley and Sons NY, 121, 1999, P 262. 21.\tSohlberg K, Pennycook S. J., Pantelides S. T., J. Am. Chem. Soc., 1999, 121, 10999. 22.\t Satterfield C. N., Heterogenous Catalysis in Practice, McGraw Hills, NY, 1980, Sect 4.5."]}
An efficient, Bi(NO3)3-Al2O3 catalyzed one pot three component synthesis of 6-amino-4-aryl-5-cyano-3-methyl-1-phenyl-1,4-dihydropyrano[2,3-c]pyrazoles via a reaction between 3-methyl-1-phenyl-2-pyrazolin-5-one, aromatic aldehydes and malononitrile is described. This method provides advantages such as high yield, shorter reaction time, mild reaction conditions, easy work-up procedure and operational simplicity.
Bi(NO3)3-Al2O3, 1,4-dihydropyrano[2,3-c]pyrazoles, One Pot Synthesis & Solid-State, Bi(NO3)3-Al2O3, 1,4-dihydropyrano[2,3-c]pyrazoles, One Pot Synthesis & Solid-State
Bi(NO3)3-Al2O3, 1,4-dihydropyrano[2,3-c]pyrazoles, One Pot Synthesis & Solid-State, Bi(NO3)3-Al2O3, 1,4-dihydropyrano[2,3-c]pyrazoles, One Pot Synthesis & Solid-State
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 0 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
| views | 2 | |
| downloads | 4 |

Views provided by UsageCounts
Downloads provided by UsageCounts