Synthesis of (-)-Muricatacin and (-)-(5R,6S)-6-acetoxy-5-hexadecanolide, the Mosquito oviposition attractant pheromone, from D-isoascorbic acid
- 3 January 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (1) , 115-118
- https://doi.org/10.1016/0040-4039(94)88177-4
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Microbial transformation of (−)-Vernolic acid into (4r,5r).5.Hydroxy-γ-decalactoneTetrahedron: Asymmetry, 1993
- Regioselective opening of chiral hydroxy epoxides: A short route to muricatacin and its diastereomer epi-muricatacinTetrahedron Letters, 1993
- Synthesis of all four isomers of disparlure using osmium-catalyzed asymmetric dihydroxylation.Tetrahedron Letters, 1992
- Muricatacin: A simple biologically active acetogenin derivative from the seeds of annona muricata (annonaceae)Tetrahedron Letters, 1991
- Synthesis of chiral epoxy alcohols: synthesis of (+)-disparlureTetrahedron Letters, 1991
- A novel carbon-carbon bond-forming reaction of triflates with copper(I)-catalyzed Grignard reagents. A new concise and enantiospecific synthesis of (+)-exo-brevicomin, (5R,6S)-(-)-6-acetoxy-5-hexadecanolide, and L-factorThe Journal of Organic Chemistry, 1990
- Inversion of configurations of contiguous carbinol centres: application to the synthesis of both enantiomers of natural products from the same enantiomerically pure starting materialCarbohydrate Research, 1990
- Synthesis of optically active pheromonesTetrahedron, 1989
- erythro-6-Acetoxy-5-hexadecanolide, the major component of a mosquito oviposition attractant pheromoneJournal of the Chemical Society, Chemical Communications, 1982
- Synthesis and activity of optically active disparlureJournal of the American Chemical Society, 1974