Cs2CO3-promoted synthesis of p-terphenyls from allyl ketones
نویسندگان
چکیده
منابع مشابه
p-Terphenyls from the basidiomycete Thelephora aurantiotincta.
A new p-terphenyl, named aurantiotinin A (1), together with ganbajunin C (2) and atromentin (3) were isolated from the fruiting bodies of the basidiomycete Thelephora aurantiotincta Corner. Their structures were established by spectral (MS, IR, UV, NMR, H-H COSY, HMQC, HMBC measurement) and chemical methods.
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Diverse p-terphenyl compounds, named curtisians, have been isolated from the fungus Paxillus curtisii, and degradation of wood by this fungus is thought to be progressed by iron chelation of p-terphenyl curtisians. In this study, the iron chelation ability of p-terphenyls has been proved by chrome azurol S (CAS) assay, reducing power, and UV-visible spectroscopic analyses. The catechol moiety o...
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The efficient synthesis has been described to achieve a new class of ladder π-conjugated molecules, B,N-bridged p-terphenyls. The bridging B atom exhibits a more significant effect than the bridging N atom on photophysical properties.
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Two novel phenylacetoxylated p-terphenyl derivatives, namely ganbajunin F (6'-methoxy-2'-phenylacetoxy-3', 4, 4", 5'-tetrahydroxy- p-terphenyl), and ganbajunin G (5'-methoxy-2'-phenylacetoxy-3', 4, 4", 6'-tetrahydroxy-p-terphenyl), together with a known compound cycloleucomelone were isolated from the fruiting bodies of Thelephora ganbajun Zang. Their structures were established on the basis of...
متن کاملIodine promoted α-hydroxylation of ketones.
A novel method for α-hydroxylation of ketones using substoichiometric amount of iodine under metal-free conditions is described. This method has been successfully employed in synthesizing a variety of heterocyclic compounds, which are useful precursors. α-Hydroxylation of diketones and triketones are illustrated. This strategy provides a novel, efficient, mild and inexpensive method for α-hydro...
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ژورنال
عنوان ژورنال: Journal of Saudi Chemical Society
سال: 2019
ISSN: 1319-6103
DOI: 10.1016/j.jscs.2018.06.009