Surprising Transformation of Azulene by Cycloaddition with 1-(Diethylamino)propyne
Author:
Publisher
Wiley
Subject
General Chemistry,Catalysis
Reference18 articles.
1. in : Non-Benzenoid Aromatic Compounds. Wiley-Interscience, New York 1959, pp. 171 ff;
2. : Molecular Orbital Theory for Organic Chemists. Wiley, New York 1961, p. 297.
3. Tetracyanoethylene and enol ethers. A model for 2 + 2 cycloadditions via zwitterionic intermediates
4. Cycloadditionsreaktionen des Pentalens und Azulens – Eine einfache Heptalen-Synthese
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1. Heptalene Synthesis by Addition of Aryl Acetylenes to Azulenes;Russian Journal of Organic Chemistry;2020-04
2. Transformation of azulenes to bicyclic [4]dendralene and heptafulvene derivatives via photochemical cycloaddition of dialkylsilylene;Chemical Communications;2015
3. Reactions of 2-Aminoazulenes with Electron-Deficient Acetylenes;Bulletin of the Chemical Society of Japan;1991-08
4. New aspects of the chemistry of nonbenzenoid polycyclic conjugated π-electron systems;Pure and Applied Chemistry;1982-01-01
5. Structure of a 1:1 adduct of 4,6,8-trimethylazulene and 1-(diethylamino)propyne;Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry;1980-03-01
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