2006
DOI: 10.1107/s1600536806033344
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1,8-Dihydroxy-3-methyl-6-(oxiran-2-ylmethoxy)-9,10-dihydroanthracene-9,10-dione

Abstract: Key indicatorsSingle-crystal X-ray study T = 296 K Mean (C-C) = 0.003 Å R factor = 0.052 wR factor = 0.169 Data-to-parameter ratio = 15.4For details of how these key indicators were automatically derived from the article, see

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“…Emodin and its derivatives have been found to possess diverse biological properties, such as antimicrobial, antiviral, antitumor, anti-inflammatory, anti-oxidant, immunosuppressive, anti-ulcerogenic, fungicidal and chemopreventive activities (Wang & Xu, 2005;Teich et al, 2004;Srinivas et al, 2003). As part of our ongoing research on emodin derivatives (Wang & Xu, 2005;Wang et al, 2006), we report here the crystal structure of the title compound.…”
Section: S1 Commentmentioning
confidence: 97%
See 1 more Smart Citation
“…Emodin and its derivatives have been found to possess diverse biological properties, such as antimicrobial, antiviral, antitumor, anti-inflammatory, anti-oxidant, immunosuppressive, anti-ulcerogenic, fungicidal and chemopreventive activities (Wang & Xu, 2005;Teich et al, 2004;Srinivas et al, 2003). As part of our ongoing research on emodin derivatives (Wang & Xu, 2005;Wang et al, 2006), we report here the crystal structure of the title compound.…”
Section: S1 Commentmentioning
confidence: 97%
“…The organic phase was washed with water (15 ml) and brine (15 ml), and dried over anhydrous sodium sulfate. The solvent was removed to give the key intermediate, 1,8-Dihydroxy-3-methyl-6-(oxiran-2-ylmethoxy)-9,10-dihydroanthracene-9,10-dione (Wang et al, 2006) as a yellow oil, which was purified by flash chromatography (silica gel, petroleum ether-acetone 3:1). To a solution of above intermediate (0.326 g, 1 mmol) in chloroform was added 2,4-dimethylaniline (1.1 mmol).…”
Section: S2 Experimentalmentioning
confidence: 99%