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Preparation of mononitropyrogallols and their methyl ethers, acetates, and benzenesulphonates

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dc.contributor.author Kampouris, EM en
dc.date.accessioned 2014-03-01T01:37:43Z
dc.date.available 2014-03-01T01:37:43Z
dc.date.issued 1971 en
dc.identifier.issn 00224952 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/21656
dc.title Preparation of mononitropyrogallols and their methyl ethers, acetates, and benzenesulphonates en
heal.type journalArticle en
heal.identifier.primary 10.1039/J39710002577 en
heal.identifier.secondary http://dx.doi.org/10.1039/J39710002577 en
heal.publicationDate 1971 en
heal.abstract Mononitration of pyrogallol 1,3- and 1,2-dibenzenesulphonate, gave 5-nitropyrogallol 1,3-dibenzenesulphonate 4-nitropyrogallol 1,2- dibenzenesulphonate and 4-nitropyrogallol 2,3-dibenzonesulphonate; these were separated and characterised. Mononitration of pyrogallol triacetate gave a mononitro-compound which was separated and characterised as the 4-nitropyrogallol 1,2-diacetate. From the above nitro-derivatives of 5-nitropyrogallol and 4-nitropyrogallol, a number of mono-, di-, and tri-methyl ethers, acetates, and benzenesulphonates were prepared. en
heal.journalName Journal of the Chemical Society C: Organic Chemistry en
dc.identifier.doi 10.1039/J39710002577 en
dc.identifier.spage 2577 en
dc.identifier.epage 2579 en


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