Abstract
A simple protocol for a regioselective cross dehydrogenative reaction of 2-aryl-quinazolinones with different phenyl carboxylic acids was developed using a palladium catalyst facilitated by C–H activation. Simple and readily accessible aromatic carboxylic acids were utilized as a source of benzoxylate. A one-pot method proceeded with great regioselectivity and offered mono benzoxylation product with moderate to excellent yield.
| Original language | English |
|---|---|
| Article number | 155214 |
| Journal | Tetrahedron Letters |
| Volume | 147 |
| DOIs | |
| State | Published - 1 Sep 2024 |
| Externally published | Yes |
Keywords
- Ceric ammonium nitrate
- Cross dehydrogenative coupling
- C–H activation
- Palladium catalysis
- Quinazolinone
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry