Hetero-diels-alder reactions of α-methoxymethylene substituted 1.3-dicarbonyl compounds with enol and enediol ethers
- 31 December 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (17) , 1789-1792
- https://doi.org/10.1016/s0040-4039(00)86742-8
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Synthesis and glycosidation reactions of acetylated racemic pseudoglycals1Carbohydrate Research, 1981
- A short synthesis of racemic uronic acids and 2,3-anhydrouronic acidsCarbohydrate Research, 1981
- Zur Kenntnis organischer Lewis‐Säuren, 34. Die thermische [4π + 2π]‐Cycloaddition von Enolethern an 1,1‐dicarbonylsubstituierte EtheneEuropean Journal of Inorganic Chemistry, 1980
- Diels-alder reactions of 2-acetyl-2-cyclohexenone with enol ethers and emaminesTetrahedron Letters, 1980
- Intramolecular reactions of 1-allylic 2,2-dimethyl ethylenetricarboxylatesJournal of the American Chemical Society, 1979
- A convenient preparation of 2,3-unsaturated N-galactosyl derivativesCarbohydrate Research, 1979
- Simple de‐novo Synthesis of Reactive Pseudoglycals (Hex‐2‐enopyranosides)—Stereospecific α‐Glycoside CouplingAngewandte Chemie International Edition in English, 1977
- Einfache de-novo-Synthese reaktiver Pseudoglykale (Hex-2-enopyranoside) – stereospezifische α-Glykosid-verknüpfungAngewandte Chemie, 1977
- Total synthesis of hexuronic acidsCarbohydrate Research, 1977
- Heterodiene syntheses with .alpha.,.beta.-unsaturated carbonyl compoundsChemical Reviews, 1975