Hrydroxyl-directed iodoetherifications of allylic alcohols. Synthesis of (±)-citreoviral.
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (21) , 2529-2532
- https://doi.org/10.1016/s0040-4039(00)98828-2
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Stereocontrol in the formation of 2,3,4-trisubstituted tetrahydrofuransTetrahedron Letters, 1984
- A new approach to c-glycoside congeners: Metal carbene mediated methylenation of aldonolactones.Tetrahedron Letters, 1984
- Stereocontrolled synthesis of trans-2,5-disubstituted tetrahydrofuransJournal of the American Chemical Society, 1984
- Stereocontrolled transformations of orthoester intermediates into substituted tetrahydrofuransJournal of the American Chemical Society, 1984
- Application of the furan carbonyl photocycloaddition reaction to the synthesis of the bis(tetrahydrofuran) moiety of asteltoxinJournal of the American Chemical Society, 1983
- Verrucosidin, a tremorgen from Penicillium verrucosum var cyclopiumJournal of the Chemical Society, Chemical Communications, 1983
- Citreoviridins from Aspergillus terreusAngewandte Chemie International Edition in English, 1980
- X-Ray crystal structure of asteltoxin, a novel mycotoxin from aspergillus stellatus curziJournal of the Chemical Society, Chemical Communications, 1979
- Structure of citreoviridin, a mycotoxin produced by penicillium citreo-viride molded on riceTetrahedron, 1977
- Aurovertin B, a metabolite of Calcarisporium arbusculaJournal of the Chemical Society, Chemical Communications, 1974