The Structure of Passifloricin A: Asymmetric Synthesis of the δ-Lactones of (2Z,5S,7R,9S,11S)- and (2Z,5R,7R,9S,11S)-Tetrahydroxyhexacos-2-enoic Acid.
✍ Scribed by Jorge Garcia-Fortanet; Juan Murga; Miguel Carda; J. Alberto Marco
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 63 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
For Abstract see ChemInform Abstract in Full Text.
📜 SIMILAR VOLUMES
Enantiocontrolled Synthesis of (11S,12S,13S)-(9Z,15Z)-and (11R,12S,13S)-(9Z,15Z)-11-Hydroxy-12,13-epoxy Octadecadienoic Acids by Means of the Sharpless Asymmetric Epoxidation of the Unsymmetrical Divinylcarbinol. -The enantioselective synthesis of the title compounds (V) and (VI), self-defensive su
Pheromone Synthesis. Part 183. Synthesis of (1R,2R,5S,7R)-and (1R,2S, 5S,7R)-2-Hydroxy-exo-brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle, Dendroctonus ponderosae. -Both title compounds (V) and (VI) are synthesized via asymmetric dihydroxylation as the key ste