Warianty tytułu
Języki publikacji
Abstrakty
Some new imidazolyl pyrazole derivatives have been synthesized using benzil, ammonium acetate, and heterocyclic aldehyde in ethanol and acetic acid under ultra sound irradiation. The obtained products using this approach are having high purity and good in yield. By conducting the reactions in ethanol, the solid products were precipitated out and could be isolated simply by filtration. The synthesized compounds were characterized by various analytical techniques such as 1H and 13C NMR and further supported by mass spectroscopy.
Słowa kluczowe
Rocznik
Tom
Strony
277--283
Opis fizyczny
Bibliogr. 27 poz., rys., tab., wz.
Twórcy
autor
- Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot - 360005, Gujarat, India. National Facility for Drug Discovery Center (NFDD), Saurashtra University Rajkot - 360005, India
autor
- Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot - 360005, Gujarat, India. National Facility for Drug Discovery Center (NFDD), Saurashtra University Rajkot - 360005, India
autor
- Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot - 360005, Gujarat, India. National Facility for Drug Discovery Center (NFDD), Saurashtra University Rajkot - 360005, India
autor
- Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot - 360005, Gujarat, India. National Facility for Drug Discovery Center (NFDD), Saurashtra University Rajkot - 360005, India , kakadiyaraja@gmail.com
autor
- Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot - 360005, Gujarat, India. National Facility for Drug Discovery Center (NFDD), Saurashtra University Rajkot - 360005, India , anamik_shah@hotmail.com
Bibliografia
- [1] P. Eilbracht, L. Barfacker, C. Buss, C. Hollmann, B.E. Kitsos-Rzychon, C. L. Kranemann, T. Rische, R. Roggenbuck, A. Schimdt, Chem. Rev. 99 (1999) 3329.
- [2] L. Weber, Drug Discov. Today 7 (2002) 143.
- [3] C. Hulme, V. Gore, Curr. Med. Chem. 10 (2003) 51.
- [4] P.A. Tempest, Curr. Opin. Drug Discov. Devel. 8 (2005) 776.
- [5] I. Ugi, Pure Appl. Chem. 73 (2001) 187.191.
- [6] A. Domling, Chem. Rev. 106 (2006) 17.
- [7] Heers J., Backx L. J., J. Mostmans, J. H. Van Cutsem J. Med. Chem. 22 (2003) 1979.
- [8] Hunkeler W., Mohler H., Pieri L., Polc, P. Bonetti, E. P. Cumin, R. Schaffner, R. Haefely, W. Nature 290 (1981) 514.
- [9] Brimblecombe R. W., Duncan W. A. M., Durant G. J., Emmett, J. C. Ganellin, C. R., Parons M. E., J. Int. Med. Res. 3 (1975) 86.
- [10] Tanigawara Y., Aoyama N., Kita T., Shirakawa K., Komada F., Kasuga M., Okumura K., Clin. Pharmacol. Ther. 66 (1999) 528.
- [11] Wauquier A., Van Den Broeck W. A. E., Verheyen J. L., Janssen P. A. J., Eur. J. Pharmacol. 47 (1978) 367.
- [12] S. Samai, G. C. Nandi, P. Singh, M. S. Singh, Tetrahedron 65 (2009) 1015.
- [13] G. V. M. Sharma, Y. Jyothi, P. S. Lakshmi, Synth. Commun. 36 (2006) 2991.
- [14] S. D. Sharma, P. Hazarika, D. Konwar, Tetrahedron Lett. 49 (2008) 2216.
- [15] S. Kantevari, S. V. N. Vuppalapati, D. O. Biradar, L. Nagarapu, J. Mol. Catal. A: Chem. 266 (2007) 109.
- [16] B. Sadeghi, B. B. F. Mirjalili, M. M. Hashemi, Tetrahedron Lett. 49 (2008) 2575.
- [17] L. Nagarapu, S. Apuri, S. Kantevari, J. Mol. Catal. A: Chem. 266 (2007) 104.
- [18] M. M. Heravi, F. Derikvand, F. F. Bamoharram, J. Mol. Catal. A: Chem. 263 (2007) 112.
- [19] S. Balalaei, A. Arabanian, Green Chem. 2 (2000) 274.
- [20] A. R. Karimi, Z. Alimohammadi, J. Azizian, A. A. Mohammadi, M. R. Mohmmadizadeh, Catal. Commun. 7 (2006) 728.
- [21] M. Kidwai, P. Mothsra, V. Bansal, R. K. Somvanshi, A. S. Ethayathulla, S. Dey, T. P. Singh, J. Mol. Catal. A: Chem. 265 (2007) 177.
- [22] A. Shaabani, A. Rahmati, J. Mol. Catal. A: Chem. 249 (2006) 246.
- [23] J. Elguero, P. Goya, N. Jagerovic and A. M. S. Silva, Targets in Heterocyclic Systems Chemistry and Properties. 6 (2002) 52.
- [24] Prakash Mehta, Prakash Davadra, Nirav Shah, Hitendra Joshi, International Letters of Chemistry, Physics and Astronomy 10 (2014) 74-80.
- [25] Prakash Mehta, Prakash Dawedra, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 11(1) (2014) 1-8.
- [26] Prakash Mehta, Prakash Davadra, Jalpa R. Pandya, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 11(2) (2014) 81-88.
- [27] Dipti L. Namera, Khushal M. Kapadiya, Mitesh M. Chhatrola, Umed C. Bhoya, International Letters of Chemistry, Physics and Astronomy 11(2) (2014) 116-126.
Uwagi
PL
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.baztech-1fa6fa38-0a67-4a54-ba23-3d3576ba2057