Abstract
A novel efficient transformation reaction of dicarboxylic acids into N-aryl-substituted azacycles is described. In this synthetic procedure, both catalytic SnCl2 and phenylsilane were used as crucial reagents for reaction of arylamines with dicarboxylic acids to produce the desired azacycles. Using this SnCl2-catalyzed synthetic method, various N-aryl-substituted azacycles were successfully prepared from arylamines with dicarboxylic acids in high yield. This practical synthetic method using catalytic SnCl2 can provide a useful approach for preparation of the desired azacycle products from many available dicarboxylic acid starting materials.
| Original language | English |
|---|---|
| Pages (from-to) | 2881-2888 |
| Number of pages | 8 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 20 |
| Issue number | 14 |
| DOIs | |
| State | Published - 2022.03.17 |
Quacquarelli Symonds(QS) Subject Topics
- Engineering - Petroleum
- Chemistry
- Biological Sciences
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