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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4872
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dc.contributor.authorHamon, David P. G.en
dc.contributor.authorTuck, Kellie Louiseen
dc.date.issued2000en
dc.identifier.citationTetrahedron, 2000; 56(27):4829-4835en
dc.identifier.issn0040-4020en
dc.identifier.urihttp://hdl.handle.net/2440/4872-
dc.descriptionAvailable online 23 June 2000.en
dc.description.abstract1-Methyl-2-cyclohexen-1-ol has been prepared by a three step synthesis from 1-methylcyclohexene, in greater than 94% e.e., via a ‘merged substitution–elimination reaction’ between NaSePh and 2-methyl-2-hydroxycyclohexyl p-toluenesulphonate.en
dc.description.statementofresponsibilityDavid P.G Hamon and Kellie L Tucken
dc.language.isoenen
dc.publisherPergamon-Elsevier Science Limiteden
dc.rightsCopyright © 2000 Elsevier Science Ltd. All rights reserved.en
dc.subjectasymmetric synthesis ; hydroxylation ; elimination reactions ; pheromonesen
dc.titleAsymmetric synthesis of (S)-1-methyl-2-cyclohexen-1-ol, a constituent of the aggregation phermone of Dendroctonus pseudotsugaeen
dc.typeJournal articleen
dc.contributor.schoolSchool of Chemistry and Physics : Chemistryen
dc.identifier.doi10.1016/S0040-4020(00)00402-6en
Appears in Collections:Chemistry publications

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