Microwave Induced Ferrier Rearrangement
- 1 August 1994
- journal article
- research article
- Published by Taylor & Francis Ltd in Synthetic Communications
- Vol. 24 (15), 2097-2101
- https://doi.org/10.1080/00397919408010221
Abstract
A short and facile entry to the 2, 3-unsaturated O-arylglyco sides via microwave induced Ferrier rearrangement of acetylated glucal is reported.Keywords
This publication has 15 references indexed in Scilit:
- Alumina-mediated cleavage ofTetrahedron Letters, 1993
- Microwave-induced organic reaction enhancement chemistry.4 convenient synthesis of enantiopure α-hydroxy-β-lactams1Tetrahedron Letters, 1992
- Reaction of 2,3-unsaturated aryl glycosides with Lewis acids : a convenient entry to C-aryl glycosidesTetrahedron Letters, 1992
- APPLICATIONS OF MICROWAVE ENERGY IN ORGANIC CHEMISTRY. A REVIEWOrganic Preparations and Procedures International, 1991
- Reactions de cycloaddition [4 + 2] sous micro - ondes des derives du glyoxalTetrahedron Letters, 1991
- Highly Accelerated Reactions in a Microwave Ovem: Synthesis of HeterocyclesHETEROCYCLES, 1990
- Palladium(0)-based approach to functionalized C-glycopyranosidesThe Journal of Organic Chemistry, 1989
- The use of microwave ovens for rapid organic synthesisTetrahedron Letters, 1986
- Application of commercial microwave ovens to organic synthesis.Tetrahedron Letters, 1986
- 712. The reaction between 3,4,6-tri-O-acetyl-D-glucal and p-nitrophenolJournal of the Chemical Society, 1962