Dienophilicity of Imidazole in Inverse Electron Demand Diels-Alder Reactions; Intramolecular Reactions with 1,2,4-Triazines.-Reference-Cited by-同舟云学术

Dienophilicity of Imidazole in Inverse Electron Demand Diels-Alder Reactions; Intramolecular Reactions with 1,2,4-Triazines.

Published:1997-10 Issue:43 Volume:38 Page:7499-7502
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Neipp Christopher E.,Ranslow Peter B.,Wan Zhaokui,Snyder John K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. Dienophilicity of Imidazole in Inverse Electron Demand Diels-Alder Reactions; Intermolecular Reactions with 1,2,4-Triazines.

2. For a review of intramolecular inverse electron demand Diels-Alder reactions: Taylor, E.C. Bull. Soc. Chim. Belg. 1988, 97, 599 – 613. For reviews of inverse electron demand Diels-Alder reactions, see ref. [1]of preceding communication.

3. See ref. [3], preceding communication.

4. Indole as a dienophile in inverse electron demand Diels-Alder reactions. 3. Intramolecular reactions with 1,2,4-triazines to access the canthine skeleton

5. Pyrrole as a dienophile in intramolecular inverse electron-demand Diels-Alder reactions with 1,2,4-triazines

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