Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/47526
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Full metadata record
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 | Petersen, Asger B. | en |
dc.contributor.author | Warren, Stuart | en |
dc.date.issued | 2006 | en |
dc.identifier.citation | Organic and Biomolecular Chemistry , 2006; 4 (16):3117-3119 | en |
dc.identifier.issn | 1477-0520 | en |
dc.identifier.uri | http://hdl.handle.net/2440/47526 | - |
dc.description | © The Royal Society of Chemistry 2006 | en |
dc.description.abstract | Treatment of 1,2-diols with diphenylphosphinoyl chloride in pyridine produces beta-chloroethyl phosphinates which react with complete control of stereochemistry to give epoxides and azido-alcohols, useful intermediates in cyclopropane synthesis. | en |
dc.description.statementofresponsibility | David J. Fox, Daniel Sejer Pedersen, Asger B. Petersen and Stuart Warren | en |
dc.publisher | Royal Society Chemistry | en |
dc.title | Diphenylphosphinoyl chloride as a chlorinating agent - The selective double activation of 1,2-diols | en |
dc.type | Journal article | en |
dc.contributor.school | School of Chemistry and Physics : Chemistry | en |
dc.identifier.doi | 10.1039/b606881b | en |
Appears in Collections: | Chemistry and Physics publications |
Files in This Item:
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hdl_47526.pdf | 139.38 kB | Publisher's PDF | View/Open |
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