A versatile and green mechanochemical route for aldehyde-oxime conversions

dc.citation.doi10.1039/c2cc36315aen_US
dc.citation.epage11291en_US
dc.citation.issue92en_US
dc.citation.jtitleChemical Communicationsen_US
dc.citation.spage11289en_US
dc.citation.volume48en_US
dc.contributor.authorAakeröy, Christer B.
dc.contributor.authorSinha, Abhijeet Shekhar
dc.contributor.authorEpa, Kanishka N.
dc.contributor.authorSpartz, Christine L.
dc.contributor.authorDesper, John
dc.contributor.authoreidaakeroyen_US
dc.contributor.authoreidsinhaen_US
dc.contributor.authoreidkanishkaen_US
dc.contributor.authoreidclspartzen_US
dc.contributor.authoreiddesperjen_US
dc.date.accessioned2012-11-26T21:58:05Z
dc.date.available2012-11-26T21:58:05Z
dc.date.issued2012-11-28
dc.date.published2012en_US
dc.description.abstractA robust, facile and solvent-free mechanochemical path for aldehyde–oxime transformations using hydroxylamine and NaOH is explored; the method is suitable for aromatic and aliphatic aldehydes decorated with a range of substituents.en_US
dc.identifier.urihttp://hdl.handle.net/2097/15045
dc.language.isoen_USen_US
dc.relation.urihttp://doi.org/10.1039/c2cc36315aen_US
dc.rightsThis Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).en_US
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectMechanochemicalen_US
dc.subjectAldehyde-oxime conversionsen_US
dc.subjectAldoximesen_US
dc.subjectHydroxylamineen_US
dc.subjectNaOHen_US
dc.titleA versatile and green mechanochemical route for aldehyde-oxime conversionsen_US
dc.typeArticle (author version)en_US

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