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3-Hydroxy-2,6-dinitroacetophenone: an unusual substitution pattern resulting from nitration of 3-hydroxyacetophenone

dc.contributor.authorCristiano, Maria Lurdes Santos
dc.contributor.authorJohnstone, Robert A. W.
dc.contributor.authorPratt, M. J.
dc.date.accessioned2014-06-06T17:47:30Z
dc.date.available2014-06-06T17:47:30Z
dc.date.issued1995
dc.date.updated2014-06-05T09:22:40Z
dc.description.abstractNitration of 3-hydroxyacetophenone gives 2,6-dinitro-3-hydroxyacetophenone, C8H6N206, in which the nitro groups have entered the sterically least favourable positions in the aromatic nucleus. None of the expected substitution in the 4-position was observed. The two nitro groups flanking the carbonyl side chain are different in that one is in the plane of the aryl ring but the other is twisted well out of the plane.por
dc.identifier.citationCristiano, M. L. S.; Johnstone, R. A. W.; Pratt, M. J. 3-Hydroxy-2,6-dinitroacetophenone: an Unusual Substitution Pattern Resulting from Nitration of 3-Hydroxyacetophenone, Acta Crystallographica Section C Crystal Structure Communications, 51, 12, 2581-2583, 1995.por
dc.identifier.issn0108-2701
dc.identifier.otherAUT: MCR00716;
dc.identifier.urihttp://hdl.handle.net/10400.1/4239
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherInternational Union of Crystallographypor
dc.title3-Hydroxy-2,6-dinitroacetophenone: an unusual substitution pattern resulting from nitration of 3-hydroxyacetophenonepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage2583por
oaire.citation.issue12por
oaire.citation.startPage2581por
oaire.citation.titleActa Crystallographica Section C Crystal Structure Communicationspor
oaire.citation.volume51por
person.familyNameCristiano
person.givenNameMaria de Lurdes
person.identifier.ciencia-idE411-6006-5A01
person.identifier.orcid0000-0002-9447-2855
person.identifier.ridG-2345-2012
person.identifier.scopus-author-id9238724800
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublicationb16751a6-748e-44b0-9c59-058cbd5b2cc3
relation.isAuthorOfPublication.latestForDiscoveryb16751a6-748e-44b0-9c59-058cbd5b2cc3

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