Lewis acid-catalyzed regiospecific opening of vinyl epoxides by alcohols
- 21 May 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (20) , 3829-3831
- https://doi.org/10.1016/s0040-4039(00)00496-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Synthesis of (−)-(4R,5R)-muricatacin using a regio- and stereospecific ring-opening of a vinyl epoxideTetrahedron Letters, 2000
- 2,3-Dichloro-5,6-Dicyano-p-Benzoquinone, an efficient, mild, neutral and highly regioselective catalyst for alcoholysis of epoxidesTetrahedron Letters, 1990
- Synthesis of the FG ring system of brevetoxin BJournal of the American Chemical Society, 1989
- Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systemsJournal of the American Chemical Society, 1989
- Tin mediated palladium catalyzed regiocontrolled alkylations of vinyl epoxidesTetrahedron Letters, 1988
- Highly regioselective ring opening of epoxides with alcohols catalyzed by organotin phosphate condensatesTetrahedron Letters, 1985
- Activation of 6-endo over 5-exo epoxide openings. Ring-selective formation of tetrahydropyran systems and stereocontrolled synthesis of the ABC ring framework of brevetoxin BJournal of the Chemical Society, Chemical Communications, 1985
- Synthesis of vinylic epoxides via arsonium ylidesTetrahedron Letters, 1983
- Organic reactions at alumina surfaces. Mild and selective opening of arene and related oxides by weak oxygen and nitrogen nucleophilesJournal of the American Chemical Society, 1977