Tungstosilicic acid (H4SiW12O40) have efficient catalysts for synthesis of 2,3-Dihydroxynaphthoquinone from lawsone

dc.contributor.authorBenferrah, Nassima
dc.contributor.authorHammadi, Mohamed
dc.contributor.authorDokari, Hadjila
dc.contributor.authorVillemin, Didier
dc.date.accessioned2018-06-04T08:07:01Z
dc.date.available2018-06-04T08:07:01Z
dc.date.issued2016
dc.description.abstractThe Thiele–Winter reaction is of interest for synthesis of tetracetoxyaromatic precursors of hydroxynaphtoquinones. Solid acids such as Tungstosilicic acid (H4 SiW12O40) have an efficient catalyst in acetoxylation reaction of naphtoquinones without the use of organic solvent at room temperature. 1,2,3,4-Tetrahydroxynaphthalene was easily oxidized at room temperature in 2,3-Dihydroxynaphthoquinone by using (Pc[Co]/K10) and air (1 atm). We have also tested this type of reaction in 2-hydroxynaphthoquinone (Lawsone). Many naphthoquinones are natural products with interesting biological propertiesen_US
dc.identifier.issn0975-413X
dc.identifier.urihttps://dspace.univ-boumerdes.dz/handle/123456789/4868
dc.language.isoenen_US
dc.relation.ispartofseriesDer Pharma Chemica/ Vol.8, N°21(2016);pp. 6-9
dc.subjectHeteropolyacidsen_US
dc.subjectWithout solventen_US
dc.subjectRoom temperatureen_US
dc.subjectLawsoneen_US
dc.subjectCatalytic system (Pc[Co]/K10)en_US
dc.titleTungstosilicic acid (H4SiW12O40) have efficient catalysts for synthesis of 2,3-Dihydroxynaphthoquinone from lawsoneen_US
dc.typeArticleen_US

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