| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5221919 | Tetrahedron | 2010 | 8 Pages |
Abstract
3-Vinylindoles as precursors of carbazole and bis-indole derivatives were synthesized. Then, to form new carbazoles, Diels-Alder reactivity of these vinylindoles was studied with various dienophiles. During the cycloaddition reaction, unusual Morita-Baylis-Hillman-type products were observed. The structure and the formation mechanism of the products is discussed.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ali Enis Sadak, Tayfun Arslan, Neslihan Celebioglu, Nurullah Saracoglu,