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231224s2013 xx |||||o 00| ||eng c |
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|a 10.1002/mrc.3937
|2 doi
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|a pubmed24n0750.xml
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|a eng
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|a Gaspar, Alexandra
|e verfasserin
|4 aut
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|a Synthesis and NMR studies of novel chromone-2-carboxamide derivatives
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|c 2013
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|a Date Completed 30.01.2014
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|a Date Revised 15.03.2013
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2013 John Wiley & Sons, Ltd.
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|a Chromones are heterocyclic compounds of natural or synthetic origin that possess relevant pharmacological activities. Versatile functionalization of the chromone nucleus allows attaining of a chemical diversity suitable to perform structure-activity relationships in drug discovery and development programs. Accordingly, the synthesis and identification of novel chromone carboxamide derivatives with electron-donating and electron-withdrawing substituents in different positions of the exocyclic ring are reported in this work. Their complete structural characterization was performed using one-dimensional and two-dimensional resonance techniques. The data acquired are useful for a prompt analysis of related compounds that encompass our integrated medicinal chemistry sketch
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|a Letter
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|a Research Support, Non-U.S. Gov't
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|a Chromones
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|a Heterocyclic Compounds
|2 NLM
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|a Cagide, Fernando
|e verfasserin
|4 aut
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1 |
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|a Quezada, Elias
|e verfasserin
|4 aut
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|a Reis, Joana
|e verfasserin
|4 aut
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|a Uriarte, Eugenio
|e verfasserin
|4 aut
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|a Borges, Fernanda
|e verfasserin
|4 aut
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|t Magnetic resonance in chemistry : MRC
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|g 51(2013), 4 vom: 15. Apr., Seite 251-4
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|g pages:251-4
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|u http://dx.doi.org/10.1002/mrc.3937
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