Studies on the acid-catalyzed opening of non-rigid: acylcyclopropanes: a dramatic solvent effect. A route to the bicyclo[2.2.1]heptane ring system
- 31 December 1974
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 15 (6) , 527-530
- https://doi.org/10.1016/s0040-4039(01)82262-0
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- A simple synthesis of (±)-cedrene and (±)-cedrol using a synchronous double annulation processTetrahedron Letters, 1973
- Olefin participation in the acid-catalyzed opening of acylcyclopropanes. IV. Cyclization of 5-methyl-6-Tetrahedron Letters, 1971
- Cyclization of epoxy olefins. VII. Attempted .pi. routes to bridged bicyclic systemsThe Journal of Organic Chemistry, 1970
- Aryl participation in concerted cyclization of cyclopropyl ketonesJournal of the American Chemical Society, 1969
- Six-membered rings via olefin participation in the opening of acylcyclopropanesJournal of the American Chemical Society, 1969
- Olefin participation in the acid-catalyzed opening of acylcyclopropanes. III. Formation of the bicyclo[2.2.1]heptane systemJournal of the American Chemical Society, 1969
- Biogenetic-type synthesis of (±)-camphorJournal of the Chemical Society D: Chemical Communications, 1969
- Die hydrolyse von phosphaten und pyrophosphaten einiger monoterpenalkoholeTetrahedron, 1967
- The Hydrolysis of Terpenyl Phosphates, Model Reactions of Terpene BiosynthesisAngewandte Chemie International Edition in English, 1965
- Solvolysis of 3-Cyclohexenylcarbinyl Derivatives1The Journal of Organic Chemistry, 1962