A versatile and green mechanochemical route for aldehyde-oxime conversions

dc.contributor.author	Aakeröy, Christer B.
dc.contributor.author	Sinha, Abhijeet S.
dc.contributor.author	Epa, Kanishka N.
dc.contributor.author	Spartz, Christine L.
dc.contributor.author	Desper, John
dc.date.accessioned	2012-11-26T21:58:05Z
dc.date.available	2012-11-26T21:58:05Z
dc.date.issued	2012-11-26
dc.identifier.uri	http://hdl.handle.net/2097/15045
dc.description.abstract	A 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.language.iso	en_US	en_US
dc.relation.uri	http://pubs.rsc.org/en/content/articlepdf/2012/cc/c2cc36315a?page=search	en_US
dc.rights	Reproduced by permission of The Royal Society of Chemistry	en_US
dc.subject	Mechanochemical	en_US
dc.subject	Aldehyde-oxime conversions	en_US
dc.subject	Aldoximes	en_US
dc.subject	Hydroxylamine	en_US
dc.subject	NaOH	en_US
dc.title	A versatile and green mechanochemical route for aldehyde-oxime conversions	en_US
dc.type	Article (author version)	en_US
dc.date.published	2012	en_US
dc.citation.doi	doi:10.1039/c2cc36315a	en_US
dc.citation.epage	11291	en_US
dc.citation.issue	92	en_US
dc.citation.jtitle	Chemical Communications	en_US
dc.citation.spage	11289	en_US
dc.citation.volume	48	en_US
dc.description.embargo	embargo 10/2013	en
dc.contributor.authoreid	aakeroy	en_US
dc.contributor.authoreid	sinha	en_US
dc.contributor.authoreid	kanishka	en_US
dc.contributor.authoreid	clspartz	en_US
dc.contributor.authoreid	desperj	en_US