Synthesis of a key intermediate for the total synthesis of streptovaricin A
- 1 January 1982
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (41) , 4199-4202
- https://doi.org/10.1016/s0040-4039(00)88703-1
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Macrolide synthesis: narbonolideThe Journal of Organic Chemistry, 1982
- Stereoselective aldol condensations via boron enolatesJournal of the American Chemical Society, 1981
- Stereoselective aldol condensation. Use of chiral boron enolatesJournal of the American Chemical Society, 1981
- Total synthesis of 6-deoxyerythronolide BJournal of the American Chemical Society, 1981
- Stereoselective iodolactonization of acyclic unsaturated 3-hydroxyacidsTetrahedron Letters, 1981
- Acyclic stereoselection. 7. Stereoselective synthesis of 2-alkyl-3-hydroxy carbonyl compounds by aldol condensationThe Journal of Organic Chemistry, 1980
- Stereoselective epoxidation of acyclic allylic alcohols. A correction of our previous work.Tetrahedron Letters, 1979
- Macrolides. Recent Progress in Chemistry and BiochemistryAngewandte Chemie International Edition in English, 1977
- Relative biological activities of individual streptovaricins and streptovaricin acetatesBiochemistry, 1974
- Structure and synthesis of dihydroxypentyluracil from bacteriophage SP-15 deoxyribonucleic acidJournal of the American Chemical Society, 1973