Inverse electron demand diels-alder reactions of 3-carbomethoxy-2-pyrones. Controlled introduction of oxygenated aromatics: benzene, phenol, catechol, resorcinol, pyrogallol annulation.-Reference-Cited by-同舟云学术

Inverse electron demand diels-alder reactions of 3-carbomethoxy-2-pyrones. Controlled introduction of oxygenated aromatics: benzene, phenol, catechol, resorcinol, pyrogallol annulation.

Published:1983-01 Issue:45 Volume:24 Page:4939-4942
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Boger Dale L.,Mullican Michael D.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Inverse electron demand diels-alder reaction of 3-carbomethoxy-2-pyrones with 1,1-dimethoxyethylene: a simple and mild method of aryl annulation

2. Regiospecific total synthesis of juncusol

3. Synthetic analgesics: preparation of racemic 6,7-benzomorphans

4. Diels-Alder synthesis of hindered aromatic amines

5. The total synthesis of ionophore antibiotics. A convergent synthesis of lasalocid A (X537A)

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