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Abstrakty
A series of 8 derivatives of chromene 5a-h synthesized via one-pot cyclocondensation reaction of N-allyl quinolones, α/β naphthol and malononitrile. And 8 derivatives of pyrimidines 8a-h bearing N-allyl quinolone have been synthesized by N-allyl quinolones, ethylacetoacetate, thiourea/urea in the presence of zinc triflate as less toxic catalyst. This methodology allowed the high conversion of product at room temperature. Titled derivatives were elucidated by FT-IR, 1H NMR, 13C NMR, elemental analysis, and mass spectral data.
Słowa kluczowe
Rocznik
Tom
Strony
199--207
Opis fizyczny
Bibliogr. 22 poz., wz.
Twórcy
autor
- Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar-388120, Gujarat, India
autor
- Present address: DSIR laboratory, Cheminova India Ltd., Panoli, Bharuch-394116, Gujarat, India
autor
- Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar-388120, Gujarat, India
Bibliografia
- [1] Kidwaia M., Poddara R., Bhardwaja S., et al., Eur. J. Med. Chem., 45 (2010) 5031-5038.
- [2] Patil A., Wang J., Li X., et al., Bioorg. Med. Chem. Lett., 22 (2012) 4458-4461.
- [3] Conti C., Monaco L., Desideri N., Bioorg. Med. Chem., 22 (2014) 1201-1207.
- [4] Johnson A., Kumar A., Rasheed S., et al., J. Ethnopharmacology, 130 (2010) 267-271.
- [5] Aggarwal R., Masan E., Kaushik P., et al., J. Fluor. Chem., 168 (2014) 16-24.
- [6] Shao K., Zhang X., Chen P., et al., Bioorg. Med. Chem Lett, 24 (2014) 3877-3881.
- [7] Desai N., Kotadiya G., Bioorg. Med. Chem. Lett, 24 (2014) 3126-3130.
- [8] Pretorius I., Breytenbach W., Kock C., et al., Bioorg. Med. Chem., 21 (2013) 269-277.
- [9] K. Kouachi, G. Lafaye, S. Pronier, L. Bennini, S. Menad, J. Mol. Catal. A: Chem., 395 (2014) 210-216.
- [10] Chaudhary G., Bansal P., Mehta S., Chem. Engineering J., 243 (2014) 217-224.
- [11] Starcevich J., Laughlin T., Mohan R., Tet. Lett., 54 (2013) 983-985.
- [12] Kalbasi R., Massah A., Daneshvarnejad B., Applied Clay Science, 55 (2012) 1-9.
- [13] Shirini F., Abedini M., Pourhasan-Kisomi R., Chin. Chem. Lett., 25 (2014) 111-114.
- [14] Nemati F., Heravi M., Rad R., Chin. J. Catalysis, 33 (2012) 1825-1831.
- [15] Shaterian H., Arman M., Rigi F., J. Mol. Liq., 158 (2011) 145-150.
- [16] Zhao X., Yang K., Zhang Y., Chin. Chem. Lett., 25 (2014) 1141-1144.
- [17] Patel N., Patel R., and Patel M., J. Environ. Res. D. 3 (2009) 851.
- [18] Jardosh H., Patel M., Eur. J. Med. Chem. 65 (2013)348-359.
- [19] Lekhok K., Bhuyan D., Prajapati D., Mol. Divers, 14 841–846.
- [20] Tsengy M., Chu Y., Tetrahedron, 64 (2008) 9515–9520.
- [21] Kumar U., Reddy S., Reddy P., et al, Tet. Lett. 55 (2014) 910–912.
- [22] Suzuki I., Suzumura Y., Takeda K., Tet. Lett. 47 (2006) 7861-7864.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-f6f00837-92c4-4474-9658-34060a6170cc