Abstract
A mild, cost-effective, and simple three-component Ugi-type reaction using p-toluenesulfinic acid (pTSIA) as the acid catalyst has been developed to synthesize α-amino amides and α-amino amidines. Employing 1 equiv of amine used in the reaction generated α-amino amides exclusively, while 2 equiv of amines, especially with more nucleophilic aniline such as p-anisidine, yielded the α-amino amidines as the major product. This methodology would be suitable for the synthesis of natural or unnatural amino acids and drug-like amidine analogues.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2340-2343 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 54 |
| Issue number | 19 |
| DOIs | |
| State | Published - May 8 2013 |
Keywords
- Amide
- Amidine
- MCR
- Three-component Ugi reaction
- p-Toluenesulfinic acid
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
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