Abstract
The hydrazide of 2-(6-methoxy α-naphthyl)-propionic acid (Naproxen) was converted to the Schiff's bases which in turn on reacting with aryl and aryloxy acetyl chlorides yielded the corresponding azetidin-2-ones (4-a-c and 5 a-t). Representative compounds screened for antitubercular activity were proved to be equipotent with streptomycin.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 221-224 |
| Number of pages | 4 |
| Journal | Indian Journal of Heterocyclic Chemistry |
| Volume | 7 |
| Issue number | 3 |
| Publication status | Published - 1998 |