New synthetic methodology utilising 1,2-dioxines and stabilised phosphorus ylides: a highly diastereoselective cyclopropanation reaction

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dc.contributor.authorAvery, T.
dc.contributor.authorHaselgrove, T.
dc.contributor.authorRathbone, R.
dc.contributor.authorTaylor, D.
dc.contributor.authorTiekink, E.
dc.date.issued1998
dc.description.abstractA new method is described for the synthesis of diastereomerically pure cyclopropanes from substituted 1,2-dioxines 1a–c and stabilised phosphorus ylides 2a–e.
dc.description.statementofresponsibilityThomas D. Avery, Thomas D. Haselgrove, Dennis K. Taylor, Edward R. T. Tiekink and Tanya J. Rathbone
dc.identifier.citationChemical Communications, 1998; 333-334(3):333-334
dc.identifier.doi10.1039/a707360g
dc.identifier.issn1359-7345
dc.identifier.issn1364-548X
dc.identifier.orcidAvery, T. [0000-0001-6882-5461]
dc.identifier.orcidTaylor, D. [0000-0002-3302-4610] [0000-0002-4274-3983] [0000-0003-0633-7424]
dc.identifier.urihttp://hdl.handle.net/2440/4414
dc.language.isoen
dc.publisherROYAL SOC CHEMISTRY
dc.source.urihttps://doi.org/10.1039/a707360g
dc.titleNew synthetic methodology utilising 1,2-dioxines and stabilised phosphorus ylides: a highly diastereoselective cyclopropanation reaction
dc.typeJournal article
pubs.publication-statusPublished

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