Optically active functionalised hydrazulenoid skeleton - via oxy-Cope rearrangement
- 4 June 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (23) , 4133-4136
- https://doi.org/10.1016/s0040-4039(98)00707-2
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Studies in bromoacetylenic oxy-Cope rearrangement: Synthesis of functionalised medium-size, bicyclic and angularly fused tricyclic compoundsTetrahedron, 1997
- Synthesis of linearly fused tricyclic compounds via thermal oxy-Cope rearrangementTetrahedron, 1996
- Stereoselective Construction of the Dicyclopenta[a,d]cyclooctene Core of the Ceroplastin Sesterterpenes by Way of the Anionic Oxy-Cope RearrangementThe Journal of Organic Chemistry, 1996
- Ring enlargement-annulation via thermal oxy-Cope rearrangementTetrahedron Letters, 1993
- Studies in base-catalyzed allenic oxy-Cope rearrangement: an expedient synthesis of functionalized bicyclo[4.3.0] and -[4.4.0] systems and 3,5-cycloundecadien-1-oneThe Journal of Organic Chemistry, 1993
- Synthetic studies targeted at the cytotoxic 8,9-seco-ent-kaurene diterpenes. Concise complementary stereocontrolled construction of the bridgehead olefin coreThe Journal of Organic Chemistry, 1989
- Catalysis of the Cope and Claisen rearrangementsChemical Reviews, 1984
- Biological activities of sesquiterpene lactonesPhytochemistry, 1976
- Picrotoxinin and Related SubstancesChemical Reviews, 1967
- A Synthesis of Ketones by the Thermal Isomerization of 3-Hydroxy-1,5-hexadienes. The Oxy-Cope RearrangementJournal of the American Chemical Society, 1964