A versatile and green mechanochemical route for aldehyde-oxime conversions
dc.citation.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.contributor.author | Aakeröy, Christer B. | |
dc.contributor.author | Sinha, Abhijeet Shekhar | |
dc.contributor.author | Epa, Kanishka N. | |
dc.contributor.author | Spartz, Christine L. | |
dc.contributor.author | Desper, John | |
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 |
dc.date.accessioned | 2012-11-26T21:58:05Z | |
dc.date.available | 2012-11-26T21:58:05Z | |
dc.date.issued | 2012-11-28 | |
dc.date.published | 2012 | en_US |
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.identifier.uri | http://hdl.handle.net/2097/15045 | |
dc.language.iso | en_US | en_US |
dc.relation.uri | http://doi.org/10.1039/c2cc36315a | en_US |
dc.rights | This 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.uri | http://rightsstatements.org/vocab/InC/1.0/ | |
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 |