Stereoselective synthesis of the functionalized -1,3,5,7-tetraol
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (36) , 3873-3876
- https://doi.org/10.1016/s0040-4039(00)94299-0
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Carbamate mediated 1,3-asymmetric induction. A stereoselective synthesis of acyclic 1,3-diol systemsTetrahedron Letters, 1982
- Carbonate extension. A versatile procedure for functionalization of acyclic homoallylic alcohols with moderate stereocontrolThe Journal of Organic Chemistry, 1982
- Synthesis of saccharides and related polyhydroxylated natural products. 2. Simple deoxyalditolsThe Journal of Organic Chemistry, 1982
- Reductive ring openings of allyl-alcohol epoxidesTetrahedron Letters, 1982
- Lewis acid catalyzed cyclocondensations of functionalized dienes with aldehydesJournal of the American Chemical Society, 1982
- Stereocontrolled synthesis of 1,3,5…(2n+ 1) polyolsJournal of the Chemical Society, Chemical Communications, 1982
- Highly stereoselective synthesis ofTetrahedron Letters, 1981
- A new regio- and stereo-selective functionalization of allylic and homoallylic alcoholsJournal of the Chemical Society, Chemical Communications, 1981
- STEREOSELECTIVE SYNTHESIS OF MESO(OR ERYTHRO) 1,3-DIOLS FROM β-HYDROXYKETONESChemistry Letters, 1980
- "Phosphate extension". A strategem for the stereoselective functionalization of acyclic homoallylic alcoholsJournal of the American Chemical Society, 1977