(2S,6S,8S)-2,8-Dimethyl-1,7-dioxaspiro[5.5]undecane: A natural spiroacetal lacking anomeric stabilisation
- 1 April 1995
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 6 (4) , 967-972
- https://doi.org/10.1016/0957-4166(95)00107-z
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Diastereo- and enantioselective routes to some 2,8-dimethyl-1,7-dioxaspiro[5.5]undecanols. Absolute stereochemistry of (E,E,E)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecan-3-ol and of (E,E)-8-methyl-1,7-dioxaspiro[5.5]undecan-2-yl)methanol present in Bactrocera cucumisThe Journal of Organic Chemistry, 1992
- Cyclization of Hydroxyenol Ethers into Spiroacetals. Evidence for the position of the transition state and its implication on the stereoelectronic effects in acetal formationHelvetica Chimica Acta, 1992
- Chemistry of fruit flies. Composition of the rectal gland secretion of (male) Dacus cucumis (cucumber fly) and Dacus halfordiae. Characterization of (Z,Z)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecaneThe Journal of Organic Chemistry, 1989
- Enhancement of optical purity of a product by removing unwanted diastereomers in the course of a chiral synthesis: new synthesis of the stereoisomers of 2,8-dimethyl-1,7-dioxaspiro[5.5]undecane, the pheromone ofTetrahedron, 1985
- Synthesis of the enantiomers of cis-2-methyl-5-hexanolide, the major component of the sex pheromone of the carpenter beeTetrahedron, 1985
- Total synthesis of the macrolide, zearalenoneTetrahedron, 1968
- Unambiguous specification of stereoisomerism about a double bondJournal of the American Chemical Society, 1968