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• W2951773810 abstract "The silica gel-catalyzed synthesis of 5-amino-2-aryl-3H-chromeno[4,3,2-de][1,6]naphthyridine-4-carbonitriles and 5-amino-2-aryl-3H-quinolino[4,3,2-de][1,6]naphthyridine-4-carbonitriles were simply achieved upon the one-pot cascade reaction of malononitrile with substituted 2-hydroxyacetophenone (or 2-aminoacetophenone) and aromatic aldehyde in aqueous media. The mechanistic investigation results based on electrospray ionization mass spectrometry (ESI-MS) indicated that malononitrile displayed a dual role during this transformation. Thirteen bonds were cleaved and 12 new bonds were constructed in the formation of 5-amino-2-aryl-3H-chromeno[4,3,2-de][1,6]naphthyridine-4-carbonitriles, while only 2 H2O molecules were removed. The fluorescence properties screening showed five new compounds have high fluorescence quantum yields." @default.
• W2951773810 created "2019-06-27" @default.
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• W2951773810 date "2009-12-21" @default.
• W2951773810 modified "2023-09-26" @default.
• W2951773810 title "Silica Gel-Catalyzed One-Pot Syntheses in Water and Fluorescence Properties Studies of 5-Amino-2-aryl-3<i>H</i>-chromeno[4,3,2-<i>de</i>][1,6]naphthyridine-4-carbonitriles and 5-Amino-2-aryl-3<i>H</i>-quinolino[4,3,2-<i>de</i>][1,6]naphthyridine-4-carbonitriles" @default.
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• W2951773810 doi "https://doi.org/10.1021/cc9001179" @default.
• W2951773810 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20025233" @default.
• W2951773810 hasPublicationYear "2009" @default.
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