Synthesis of both the enantiomers of erythro-6-acetoxy-5-hexadecanolide
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 39 (20) , 3267-3269
- https://doi.org/10.1016/s0040-4020(01)91574-1
Abstract
No abstract availableFunding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 6 references indexed in Scilit:
- erythro-6-Acetoxy-5-hexadecanolide, the major component of a mosquito oviposition attractant pheromoneJournal of the Chemical Society, Chemical Communications, 1982
- Synthesis of the two enantiomeric forms of erythro-6-acetoxy-5-hexadecanolide, the major component of a mosquito oviposition attractant pheramoneJournal of the Chemical Society, Chemical Communications, 1982
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 1981
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981
- Copper-catalysed reactions of grignard reagents with epoxides and oxetane.Tetrahedron Letters, 1979
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973