Regio- and stereoselective ring opening of epoxy alcohols with organoaluminium compounds leading to 1,2-diols
- 1 January 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (35), 3597-3600
- https://doi.org/10.1016/s0040-4039(00)87680-7
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Virginiamycin M: absolute configuration and synthetic studesTetrahedron Letters, 1982
- Synthesis of saccharides and related polyhydroxylated natural products. 2. Simple deoxyalditolsThe Journal of Organic Chemistry, 1982
- Synthesis of saccharides and related polyhydroxylated natural products. 1. Simple alditolsThe Journal of Organic Chemistry, 1982
- Stereocontrolled synthesis of D-pentitols, 2-amino-2-deoxy-D-pentitols and 2-deoxy-D-pentitols from D-glyceraldehyde acetonideJournal of the American Chemical Society, 1982
- Regioselektive Öffnung von α- und β-Alkoxyepoxiden mit Trimethylaluminium†Angewandte Chemie International Edition in English, 1982
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 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
- Specific directing effects in the opening of vicinal hydroxy epoxidesThe Journal of Organic Chemistry, 1977