Cleavage of the silicon-carbon bond by fluoride ion in triorganosilyloxiranes. The stereochemistry of substitution at oxiranyl carbon.
- 1 July 1976
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 17 (31), 2667-2670
- https://doi.org/10.1016/s0040-4039(00)77790-2
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Entry into the allene oxide-cyclopropanone system via vinylsilanesTetrahedron Letters, 1974
- Cleavage of the silicon-vinyl carbon bond by fluoride ion: An unexpected β-hydroxy effectTetrahedron Letters, 1974
- The synthesis of alkenes from carbonyl compounds and carbanions alpha to silicon, II: 1,2-alkadienesTetrahedron Letters, 1974
- Conjugate addition of ditrimethylsilylvinyl cuprates: protected acyl anion enolate carbanion equivalents.Tetrahedron Letters, 1974
- Preferred conformation of the isobutyl, cyclopropylcarbinyl, and oxirylcarbinyl cations, radicals, and anions as determined by semiempirical intermediate neglect of differential orbital calculationsJournal of the American Chemical Society, 1972
- New synthesis of aldehydes via vinylsilanesJournal of the American Chemical Society, 1971
- Epoxidation of allylic alcohols with peroxy-acids. Attempts to define transition state geometryJournal of the Chemical Society B: Physical Organic, 1970
- Determination of erythro and threo configurations by nuclear magnetic resonance spectroscopyCanadian Journal of Chemistry, 1968
- The cleavage of ethynylsilanes by alcoholic solutions of alkali halidesJournal of Organometallic Chemistry, 1967
- Stereochemical studies. VI. Configuration of the 1-phenylpropane-1,2-diols; Steric course of the hydrolysis of cis- and trans-1-phenyl-2-methylethyleneoxideCollection of Czechoslovak Chemical Communications, 1955