Activation of the Dienophilicity of Indoles in Normal Electron Demand [4 + 2] Cycloadditions under High Pressure-Reference-Cited by-同舟云学术

Activation of the Dienophilicity of Indoles in Normal Electron Demand [4 + 2] Cycloadditions under High Pressure

Published:2001-02-01 Issue:4 Volume:3 Page:515-518
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chataigner Isabelle¹,Hess Elisabeth¹,Toupet Loïc¹,Piettre Serge R.¹

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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