Adelaide Research & Scholarship
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https://hdl.handle.net/2440/4872
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| Type: | Journal article |
| Title: | Asymmetric synthesis of (S)-1-methyl-2-cyclohexen-1-ol, a constituent of the aggregation phermone of Dendroctonus pseudotsugae |
| Author: | Hamon, David P. G. Tuck, Kellie Louise |
| Citation: | Tetrahedron, 2000; 56(27):4829-4835 |
| Publisher: | Pergamon-Elsevier Science Limited |
| Issue Date: | 2000 |
| ISSN: | 0040-4020 |
| School/Discipline: | School of Chemistry and Physics : Chemistry |
| Statement of Responsibility: | David P.G Hamon and Kellie L Tuck |
| Abstract: | 1-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. |
| Keywords: | asymmetric synthesis ; hydroxylation ; elimination reactions ; pheromones |
| Description: | Available online 23 June 2000. |
| Rights: | Copyright © 2000 Elsevier Science Ltd. All rights reserved. |
| DOI: | 10.1016/S0040-4020(00)00402-6 |
| Appears in Collections: | Chemistry publications |
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