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International Letters of Chemistry, Physics and Astronomy
Volume 47
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Zinc Triflate Promoted General Synthetic Protocol for the Facile Construction of Chromenes and Pyrimidines Bearing N-Allyl Quinolone Nucleus
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Zinc Triflate Promoted General Synthetic Protocol for the Facile Construction of Chromenes and Pyrimidines Bearing N-Allyl Quinolone Nucleus

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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:
February 2015
Authors:
Nileshkumar D. Vala, Hardik H. Jardosh, Manish P. Patel
Keywords:
Chromenes, N-Ally Quinolone, Pyrimidines, Zinc Triflate
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Distribution:
Open Access

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

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