A Short, Efficient, Multigram Synthetic Route to 2,3-Dimethylfuran and Some of its 2-Substituted Derivatives
- 1 April 1990
- journal article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 20 (8) , 1113-1123
- https://doi.org/10.1080/00397919008052818
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Model reactions on roast aroma formationZeitschrift für Lebensmittel-Untersuchung und Forschung, 1987
- Synthesis of both the enantiomers of the heterocyclic pheromones isolated from the male swift moth lTetrahedron, 1986
- Total synthesis of (.+-.)-tirandamycin AJournal of the American Chemical Society, 1985
- Furans as intermediates for the synthesis of oxygenated natural products. A formal asymmetric synthesis of (+)-tirandamycic acidThe Journal of Organic Chemistry, 1984
- Acyclic stereocontrol via the claisen rearrangement: a formal synthesis of (+) tirandamycic acidTetrahedron Letters, 1984
- Stereocontrolled General Synthesis of Pyrimidine C-Nucleosides Having Branched-chain Sugar MoietiesBulletin of the Chemical Society of Japan, 1983
- Total synthesis of tirandamycin. A short, efficient synthesis of the Ireland alcoholThe Journal of Organic Chemistry, 1983
- Preparation of 2,9-dioxabicyclo[3.3.1]nonanes. A model for tirandamycinTetrahedron Letters, 1982
- A practical synthesis of 2,3‐dimethylfuran and an efficient stereoselective preparation of z‐3‐methyl‐2‐pentene‐1,4‐diolJournal of Heterocyclic Chemistry, 1975
- Synthese von 2,3‐ und 3,4‐DimethylfuranHelvetica Chimica Acta, 1933