(1S,2R,8aS)-1,2-Dihydroxyindolizidine formation by Rhizoctonia leguminicola, the fungus that produces slaframine and swainsonine
- 1 July 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 52 (14), 3094-3098
- https://doi.org/10.1021/jo00390a024
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Total synthesis of (−)-swainsonine, an α-d-mannosidase inhibitor isolated from Swainsona canescensCarbohydrate Research, 1985
- The similar effects of swainsonine and locoweed on tissue glycosidases and oligosaccharides of the pig indicate that the alkaloid is the principal toxin responsible for the induction of locoismArchives of Biochemistry and Biophysics, 1984
- The synthesis and biological activity of (±)-(1α,2α,8α)-Indolizidine-1,2-diolAustralian Journal of Chemistry, 1984
- (1S,2R,8R,8aR)-1,2,8-trihydroxyoctahydroindolizine (swainsonine), an α-mannosidase inhibitor from Rhizoctonia leguminicolaTetrahedron, 1983
- Loco Intoxication: Indolizidine Alkaloids of Spotted Locoweed ( Astragalus lentiginosus )Science, 1982
- Inhibition of lysosomal α-mannosidase by swainsonine, an indolizidine alkaloid isolated from Swainsona canescensBiochemical Journal, 1980
- Crystal structure of swainsonine diacetateAustralian Journal of Chemistry, 1980
- Biosynthesis of slaframine, (1S,6S,8aS)-1-acetoxy-6-aminooctahydroindolizine, parasympathomimetic alkaloid of fungal origin. 4. Metabolic fate of ethyl pipecolylacetate, 1,3-dioxooctahydroindolizine, and 1-hydroxyoctahydroindolizine in Rhizoctonia leguminicolaBiochemistry, 1979
- Biosynthesis of slaframine, (1S,6S,8aS)-1-acetoxy-6-aminooctahydroindolizine, parasympathomimetic alkaloid of fungal origin. 3. Origin of the pyrrolidine ringBiochemistry, 1979
- LYSOSOMAL STORAGE IN SWAINSONA SPP. TOXICOSIS: AN INDUCED MANNOSIDOSISNeuropathology and Applied Neurobiology, 1978