Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
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
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

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.