| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271925 | Tetrahedron Letters | 2013 | 5 Pages |
Abstract
A general and efficient reaction of indole with oxalyl chloride and nucleophiles providing indole-3-glyoxyl derivatives has been developed in mild conditions. In the same fashion, the other reaction involved the addition of organic azides leading to the synthesis of indole-3-glyoxyl-1,2,3-triazoles, which proceeds smoothly generating the products in moderate to high yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
