Azulene analogues of triphenylmethyl cation; extremely stable hydrocarbon carbocations
- 1 February 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (6) , 773-776
- https://doi.org/10.1016/s0040-4039(00)74883-0
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Nonlinear optical properties of organic molecules. 7. Calculated hyperpolarizabilities of azulenes and sesquifulvaleneJournal of the American Chemical Society, 1988
- Autoxidation of azulene in aprotic polar solvents.NIPPON KAGAKU KAISHI, 1988
- 1,2:3,4:5,6-Tris(bicyclo[2.2.2]octeno)tropylium ion: an all-hydrocarbon carbocation with extraordinary stabilityJournal of the American Chemical Society, 1988
- Cyclopropyl/phenylcyclopropenyl cations: studies in stabilizationJournal of the American Chemical Society, 1986
- The tricyclopropylcyclopropenyl cationTetrahedron Letters, 1980
- The tricyclopropylcyclopropenium ionTetrahedron Letters, 1980
- Fulvenes and thermochromic ethylene. 88. Stabilization of cyclopropenium ion and cyclopropenone by guaiazuleneThe Journal of Organic Chemistry, 1976
- Substituent effects on cyclopropenium ionsJournal of the American Chemical Society, 1973
- Zur Kenntnis der Azulene, VII. 1‐bzw. 3‐Alkyliden‐azulenium‐SalzeEuropean Journal of Organic Chemistry, 1961
- Azulene. VIII. A Study of the Visible Absorption Spectra and Dipole Moments of Some 1- and 1,3-Substituted Azulenes1,2Journal of the American Chemical Society, 1959