Regioselective opening of 2,3-epoxy alcohols with organocuprates. Enhanced C-2 selectivity through solvent effects.
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (42) , 5009-5012
- https://doi.org/10.1016/s0040-4039(00)96682-6
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Diastereoselective synthesis of (24R,25S)-5.beta.-cholestane-3.alpha.,24,26-triolThe Journal of Organic Chemistry, 1987
- Asymmetric Epoxidation of Allylic Alcohols: The Sharpless EpoxidationSynthesis, 1986
- Copper(I)-catalyzed reactions of .beta.,.gamma.-epoxy alcohols with Grignard reagentsThe Journal of Organic Chemistry, 1983
- Stereo and regioselective openings of chiral 2,3-epoxy alcohols. Versatile routes to optically pure natural products and drugs. Unusual kinetic resolutionsPure and Applied Chemistry, 1983
- Regioselectivity of the reactions of trialkylaluminum reagents with 2,3-epoxyalcohols: Application to the synthesis of α-chiral aldehydesTetrahedron Letters, 1983
- Virginiamycin M: absolute configuration and synthetic studesTetrahedron Letters, 1982
- Regio- and stereoselective ring opening of epoxy alcohols with organoaluminium compounds leading to 1,2-diolsTetrahedron Letters, 1982
- Further synthetic studies on rifamycin sTetrahedron, 1981
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- Stereo- and regioselective methods for the synthesis of three consecutive asymmetric units found in many natural productsTetrahedron Letters, 1979