Stereo- and regio-controlled aldol synthesis
- 31 December 1980
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 21 (44), 4291-4294
- https://doi.org/10.1016/s0040-4039(00)92886-7
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Base-induced rearrangement of 1-trimethylsilylpropargyl alcohol. Generation of lithiated trimethylsiloxyallenes and their reactionsTetrahedron Letters, 1980
- Stereo- and regio-selective conversion of 1-trimethylsilylallylic alcohols into the silyl enol ethers catalyzed by butyllithiumTetrahedron Letters, 1980
- Acyclic stereoselection. 8. A new class of reagents for the highly stereoselective preparation of threo-2-alkyl-3-hydroxycarboxylic acids by the aldol condensationThe Journal of Organic Chemistry, 1980
- Acyclic stereoselection. 7. Stereoselective synthesis of 2-alkyl-3-hydroxy carbonyl compounds by aldol condensationThe Journal of Organic Chemistry, 1980
- Regio- and Stereoselective Cross-aldol Reactions via Dialkylboryl TriflatesBulletin of the Chemical Society of Japan, 1980
- Stereoselective synthesis of β-hydroxy-α-methylketones viaTetrahedron Letters, 1979
- Use of the
E-vinyloxyborane derived from S-phenyl propanethioate for stereospecific aldol-type condensation. A simplified synthesis of the prelog-djerassi lactonic acid Tetrahedron Letters, 1979 - Stereoselective aldol condensations via boron enolatesJournal of the American Chemical Society, 1979
- Stereoselective synthesis of threo-3-hydroxy-2-methylcarboxylic acids using alkoxyalkyl propionatesJournal of the American Chemical Society, 1979
- 1-Trimethylsilylallylic alcohols as homoenolate precursors. Stereo- and regio-specific synthesis of silyl enol ethersJournal of the Chemical Society, Chemical Communications, 1979