| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5286396 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
An efficient route to a new class of indole derivatives, tetrahydrochromeno[2,3-b]carbazoles, has been developed. The cycloaddition reactions of chromone-3-carboxaldehydes with indole-o-quinodimethane gave a diastereomeric mixture of Diels-Alder cycloadducts in good yields after in situ deformylation.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Chromone-3-carboxaldehydes in Diels-Alder reactions with indole-o-quinodimethane. Synthesis of tetrahydrochromeno[2,3-b]carbazoles](/preview/png/5286396.png "First Page Preview: Chromone-3-carboxaldehydes in Diels-Alder reactions with indole-o-quinodimethane. Synthesis of tetrahydrochromeno[2,3-b]carbazoles")
Authors
M. Terzidis, C.A. Tsoleridis, J. Stephanidou-Stephanatou,