Rearrangement of 3,3-ethylenedioxy-isobornyl tosylate: an efficient new synthesis of 7-ketocamphene
- 1 January 1979
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 35 (4) , 527-530
- https://doi.org/10.1016/0040-4020(79)80150-7
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Ions α-cetocarbeniumTetrahedron, 1978
- Alternative total synthesis of (±)-β-santalene, (±)-epi-β-santalene, (±)-α-santalene, (±)-copacamphor and (±)-ylangocamphorTetrahedron Letters, 1972
- Involvement of oxygenated functions in the acetolysis of 7-oxygenated norbornyl tosylatesJournal of the American Chemical Society, 1969
- Solvolysen von 9-Keto-bicyclo(3.3.1)nonyl-2-endo-tosylat und 8-Keto-bicyclo(3.2.1)-octyl-2-endo-tosylatTetrahedron Letters, 1968
- Organic reactions in a solid matrix—ITetrahedron, 1968
- Transformations of camphorTetrahedron, 1968
- The Synthesis and Solvolysis of 7-Ketonorbornyl Tosylates1Journal of the American Chemical Society, 1966
- Biogenetic-type transformations in diterpenoidsTetrahedron Letters, 1966
- Standardization of Silicic Acid for ChromatographyAnalytical Chemistry, 1961
- Reactivity of 7-Substituted Camphenes. Structure of β-IsocamphorJournal of the American Chemical Society, 1958