A kinetic study of the thermal rearrangement of 2-(trifluoromethyl)-1-vinylcyclopropane
- 1 February 1995
- journal article
- Published by Elsevier in Journal of Fluorine Chemistry
- Vol. 70 (2) , 249-253
- https://doi.org/10.1016/0022-1139(94)03107-b
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- The thermal conversions of 6,6-difluorobicyclo[3.1.0]hex-2-enes to fluorobenzenes. An interesting dichotomy of mechanismsTetrahedron, 1992
- Evidence for a dominant suprafacial-inversion pathway in the thermal unimolecular vinylcyclopropane to cyclopentene 1,3-sigmatropic shiftJournal of the American Chemical Society, 1991
- The thermal conversion of 6,6-Difluorobicyclo[3.1.0]hex-2-ene to fluorobenzene. A novel mechanismTetrahedron Letters, 1991
- Stereochemistry of the thermal isomerization of trans-1-ethenyl-2-methylcyclopropane to 4-methylcyclopenteneJournal of the American Chemical Society, 1991
- Kinetic and thermodynamic effects in the thermal electrocyclic ring-openings of 3-fluorocyclobutene, 3,3-difluorocyclobutene, and 3-(trifluoromethyl)cyclobuteneJournal of the American Chemical Society, 1990
- Thermal rearrangements of bicyclo[3.1.0]hex-2-ene. Degenerate rearrangementsJournal of the American Chemical Society, 1974
- The effects of methoxyl and phenyl substituents on the thermal rearrangements of vinylcyclopropaneTetrahedron Letters, 1973
- Conformational control of stereochemistry in the non-concerted, degenerate rearrangement of a vinylcyclopropaneTetrahedron, 1971
- The Stereochemical Fate of the Cyclopropyl Ring in the Vinylcyclopropane RearrangementJournal of the American Chemical Society, 1967
- 1068. The thermal unimolecular isomerizations of cis- and trans-1-methyl-2-vinylcyclopropanesJournal of the Chemical Society, 1964