2018
DOI: 10.1107/s2414314618011380
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3-Hydroxy-2-(4-methylphenyl)-4H-chromen-4-one

Abstract: Our work in the area of carbon-monoxide-releasing molecules led to the synthesis and crystallization of new flavone derivatives as intermediates. Herein we report the first crystal structure of the title compound, C16H12O3, a hydroxy-substituted flavone where the 2-phenyl group has been replaced by a p-tolyl group. The introduction of the 3-hydroxy group allows the formation of intermolecular O—H...O=C hydrogen bonds, used to build centrosymmetric R 2 2(10) ring motifs in th… Show more

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Cited by 4 publications
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“…HToC solution at 0.05% (w/v) was prepared in an ethanolic medium. The reagent shown in Figure was prepared by a synthetic process analogous to the AFO reaction , and has been characterized for its purity before use by different spectroscopic techniques including IR, 1 H NMR, and 13 C NMR and the experimental melting point (M.Pt.) (Supporting Information).…”
Section: Methodsmentioning
confidence: 99%
“…HToC solution at 0.05% (w/v) was prepared in an ethanolic medium. The reagent shown in Figure was prepared by a synthetic process analogous to the AFO reaction , and has been characterized for its purity before use by different spectroscopic techniques including IR, 1 H NMR, and 13 C NMR and the experimental melting point (M.Pt.) (Supporting Information).…”
Section: Methodsmentioning
confidence: 99%