Activation of the Dienophilicity of Indoles in Normal Electron Demand [4 + 2] Cycloadditions under High Pressure
Author:
Affiliation:
1. Laboratoire des Fonctions Azotées et Oxygénées Complexes, UMR 6014 CNRS, Université de Rouen-IRCOF, Rue Tesnière, F-76821 Mont Saint Aignan, France, and Université Rennes I, UMR 6626 CNRS, Campus de Beaulieu (A11), F-35042 Rennes Cedex, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0067989
Reference23 articles.
1. Addition-rearrangement reactions of halogenated thiophene dioxides with furans
2. Indole as a dienophile in inverse electron demand Diels-Alder reactions. 5H-Pyridazino[4,5-b]indoles as cycloadducts with 3,6-dicarbomethoxy-1,2,4,5-tetrazine
3. Photochemically induced radical-cation Diels-Alder reaction of indole and electron-rich dienes
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