Paper Titles in Periodical
International Letters of Chemistry, Physics and Astronomy
Volume 47

Subscribe

Subscribe to our Newsletter and get informed about new publication regulary and special discounts for subscribers!

ILCPA > Volume 47 > Zinc Triflate Promoted General Synthetic Protocol...
< Back to Volume

Zinc Triflate Promoted General Synthetic Protocol for the Facile Construction of Chromenes and Pyrimidines Bearing N-Allyl Quinolone Nucleus

Full Text PDF

Abstract:

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.

Info:

Periodical:
International Letters of Chemistry, Physics and Astronomy (Volume 47)
Pages:
199-207
DOI:
https://doi.org/10.18052/www.scipress.com/ILCPA.47.199
Citation:
N. D. Vala et al., "Zinc Triflate Promoted General Synthetic Protocol for the Facile Construction of Chromenes and Pyrimidines Bearing N-Allyl Quinolone Nucleus", International Letters of Chemistry, Physics and Astronomy, Vol. 47, pp. 199-207, 2015
Online since:
Feb 2015
Authors:
Nileshkumar D. Vala, Hardik H. Jardosh, Manish P. Patel
Keywords:
Chromenes, N-Ally Quinolone, Pyrimidines, Zinc Triflate
Export:
RIS, BibTeX, Text
Distribution:
Open Access

Creative Commons License
This work is licensed under a
Creative Commons Attribution 4.0 International License

References:

Kidwaia M., Poddara R., Bhardwaja S, et al., Eur. J. Med. Chem., 45 (2010) 5031-5038.

Patil A., Wang J., Li X., et al., Bioorg. Med. Chem. Lett., 22 (2012) 4458-4461.

Conti C., Monaco L., Desideri N., Bioorg. Med. Chem., 22 (2014) 1201-1207.

Johnson A., Kumar A., Rasheed S., et al., J. Ethnopharmacology, 130 (2010) 267-271.

Aggarwal R., Masan E., Kaushik P, et al., J. Fluor. Chem., 168 (2014) 16-24.

Shao K., Zhang X., Chen P, et al., Bioorg. Med. Chem Lett, 24 (2014) 3877-3881.

Desai N., Kotadiya G., Bioorg. Med. Chem. Lett, 24 (2014) 3126-3130.

Pretorius I., Breytenbach W., Kock C., et al., Bioorg. Med. Chem., 21 (2013) 269-277.

K. Kouachi, G. Lafaye, S. Pronier, L. Bennini, S. Menad, J. Mol. Catal. A: Chem., 395 (2014) 210-216.

Chaudhary G., Bansal P., Mehta S., Chem. Engineering J., 243 (2014) 217-224.

Starcevich J., Laughlin T., Mohan R., Tet. Lett., 54 (2013) 983-985.

Kalbasi R., Massah A., Daneshvarnejad B., Applied Clay Science, 55 (2012) 1-9.

Shirini F., Abedini M., Pourhasan-Kisomi R., Chin. Chem. Lett., 25 (2014) 111-114.

Nemati F., Heravi M., Rad R., Chin. J. Catalysis, 33 (2012) 1825-1831.

Shaterian H., Arman M., Rigi F., J. Mol. Liq., 158 (2011) 145-150.

Zhao X., Yang K., Zhang Y., Chin. Chem. Lett., 25 (2014) 1141-1144.

Patel N., Patel R., and Patel M., J. Environ. Res. D. 3 (2009) 851.

Jardosh H, Patel M., Eur. J. Med. Chem. 65 (2013)348-359.

Lekhok K., Bhuyan D., Prajapati D., Mol. Divers, 14 841-846.

Tsengy M., Chu Y., Tetrahedron, 64 (2008) 9515-9520.

Kumar U., Reddy S., Reddy P., et al, Tet. Lett. 55 (2014) 910-912.

Suzuki I., Suzumura Y., Takeda K., Tet. Lett. 47 (2006) 7861-7864. ( Received 29 January 2015; accepted 12 February 2015 ).

Show More Hide