Bicyclic intermediates for trichothecane synthesis. Exploitation of an enolate as a protecting group.
- 31 December 1973
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 14 (48), 4807-4810
- https://doi.org/10.1016/s0040-4039(01)87342-1
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Organocopper chemistry. Halo-, cyano-, and carbonyl-substituted ketones from the corresponding acyl chlorides and organocopper reagentsJournal of the American Chemical Society, 1972
- Metal enolates as protecting groups for ketones during metal hydride reductionJournal of the Chemical Society, Chemical Communications, 1972
- The decarboxylative elimination reaction of a β,γ-epoxyacid. A route to allylic alcoholsTetrahedron Letters, 1971
- Applications of the intramolecular nuclear Overhauser effect in structural organic chemistryChemical Reviews, 1971
- Pyranosiduloses. II. The synthesis and properties of some alkyl 2,3-dideoxy-2-enopyranosid-4-ulosesCanadian Journal of Chemistry, 1970
- Stereoselective synthesis of (±)-eremophil-3,11-diene and related compounds. Concerning the structure of eremophileneCanadian Journal of Chemistry, 1969