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https://hdl.handle.net/2440/47529
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DC Field | Value | Language |
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dc.contributor.author | Fox, David J. | en |
dc.contributor.author | Pedersen, Daniel Sejer | en |
dc.contributor.author | Warren, Stuart | en |
dc.date.issued | 2004 | en |
dc.identifier.citation | Chemical Communications, 2004; 10 (22):2598-2599 | en |
dc.identifier.issn | 1359-7345 | en |
dc.identifier.uri | http://hdl.handle.net/2440/47529 | - |
dc.description | © Royal Society of Chemistry 2008 | en |
dc.description.abstract | Products of difficult ketone alkylation reactions can be made selectively via activation with a diphenylphosphinoyl group; subsequent dephosphinoylation is easily achieved in base. | en |
dc.description.statementofresponsibility | David J. Fox, Daniel Sejer Pedersen and Stuart Warren | en |
dc.publisher | Royal Society of Chemistry | en |
dc.subject | ketones (benzene compounds) | en |
dc.title | A simple, general and efficient ketone synthesis via alkylation and dephosphinoylation of β-keto-diphenylphosphine oxides | en |
dc.title.alternative | A simple, general and efficient ketone synthesis via alkylation and dephosphinoylation of beta-keto-diphenylphosphine oxides | en |
dc.type | Journal article | en |
dc.contributor.school | School of Chemistry and Physics : Chemistry | en |
dc.identifier.doi | 10.1039/b410144h | en |
Appears in Collections: | Chemistry and Physics publications |
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