| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273415 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
A series of novel tetrahydroquinolines have been synthesized via the acid-catalyzed reaction of an azaflavan-4-ol with a variety of reactive nucleophiles. The tetrahydroquinolines were found to undergo oxidation in the presence of iodine as catalyst to generate the corresponding novel 2,4-disubstituted quinolines.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
