An AMI study of the cope rearrangements of bullvalene, barbaralane, semibullvalene, and derivatives of semibullvalene
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 44 (5), 1351-1358
- https://doi.org/10.1016/s0040-4020(01)85913-5
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Alternative transition states in the Cope rearrangements of hexa-1,5-dieneJournal of the Chemical Society, Chemical Communications, 1987
- Bicyclic, boatlike Cope rearrangements. Probe for conformational preference by the nodal carbon atomsJournal of the American Chemical Society, 1985
- Ab initio calculation of the transition state for the Cope rearrangementJournal of the American Chemical Society, 1984
- Thermal rearrangements of gem-difluorocyclopropanesAccounts of Chemical Research, 1981
- Variable transition state structure in 3,3-sigmatropic shifts from .alpha.-secondary deuterium isotope effectsJournal of the American Chemical Society, 1979
- The mechanism of the Cope rearrangementJournal of the American Chemical Society, 1978
- 2,6-Substituted homotropilidenes. Influence of substituents on valence topomerizationJournal of the American Chemical Society, 1976
- Boat and chair transition states of 1,5-hexadieneJournal of the American Chemical Society, 1972
- The Introduction of Substituted Vinyl Groups. V. A Rearrangement Involving the Migration of an Allyl Group in a Three-Carbon System1Journal of the American Chemical Society, 1940
- The activation energy of diene association reactionsTransactions of the Faraday Society, 1938