Trapping of the 1,4‐Dipole Formed in the 2 + 2‐Cycloaddition of Tetracyanoethylene to Enol Ethers
- 1 January 1974
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 13 (1) , 80-81
- https://doi.org/10.1002/anie.197400801
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Nonstereospecificity in the [2 + 2] cycloadditions of tetracyanoethylene to enol ethersJournal of the American Chemical Society, 1973
- Tetracyanoethylene and enol ethers. Dependence of cycloaddition rat on solvent polarityJournal of the American Chemical Society, 1973
- Reversibility of zwitterion formation in the [2 + 2] cycloaddition of tetracyanoethylene to enol ethersJournal of the American Chemical Society, 1973
- Centenary Lecture. Mechanisms of cycloadditionQuarterly Reviews, Chemical Society, 1970
- Lösungsmitteleinflüsse bei nucleophilen aromatischen SubstitutionenEuropean Journal of Inorganic Chemistry, 1964
- Über Pyridinium‐N‐phenol‐betaine und ihre Verwendung zur Charakterisierung der Polarität von LösungsmittelnEuropean Journal of Organic Chemistry, 1963
- Cyanocarbon Chemistry. XIX.1,2 Tetracyanocyclobutanes from Tetracyanoethylene and Electron-rich AlkenesJournal of the American Chemical Society, 1962