Rearrangement of a hindered allylic alcohol during vanadium-catalyzed epoxidation. A short synthesis of uvidin-c.
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (48), 5875-5878
- https://doi.org/10.1016/s0040-4039(00)98250-9
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- A C6, C7 Oxygen Functionalized Intermediate for the Synthesis of Forskolin: Stereochemical Control in an Intramolecular Diels-Alder ReactionTetrahedron Letters, 1985
- Syntheses of the insect antifeedant (.+-.)-cinnamodial and the drimane sesquiterpenoids (.+-.)-isodrimenin and (.+-.)-fragrolideThe Journal of Organic Chemistry, 1985
- Stereospecific transformation of grindelic acid into the antifeedant 6.alpha.-hydroxygrindelic acid, its 6.beta.-epimer, and other related natural diterpene acidsThe Journal of Organic Chemistry, 1984
- TOTAL SYNTHESIS OF 6-OXO-GRINDELIC ACID METHYL ESTERChemistry Letters, 1983
- Fungal metabolites. Part 15. Structure and chemical correlations of uvidin C, D, and E, new drimane sesquiterpenes from Lactarius uvidus FriesJournal of the Chemical Society, Perkin Transactions 1, 1983
- Stereospecific total synthesis of ajugarin-IVTetrahedron Letters, 1982
- Reactions of forskolin, a biologically active diterpenoid from Coleus forskohliiJournal of the Chemical Society, Perkin Transactions 1, 1982
- Fungal metabolites. Part 5. Uvidins, new drimane sesquiterpenes from Lactarius uvidus FriesJournal of the Chemical Society, Perkin Transactions 1, 1980
- Structures and stereochemistry of new labdane diterpiniods from coleus forskohlii briq.Tetrahedron Letters, 1977
- The Stereochemistry of Polyene CyclizationJournal of the American Chemical Society, 1955