A novel synthesis of 3-halo-2-phenylquinoline-4-carboxylic acids
✍ Scribed by Luca F. Raveglia; Giuseppe A. M. Giardina; Mario Grugni; Roberto Rigolio; Carlo Farina
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 260 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The 3‐chloro and 3‐bromo‐2‐phenylquinoline‐4‐carboxylic acids were obtained in good yields through a novel procedure, entailing the synthesis of the 3‐amino intermediate and the subsequent replacement of the amino group with chlorine or bromine, according to the Sandmeyer reaction.
📜 SIMILAR VOLUMES
## Abstract magnified image A series of twelve substituted 2‐phenylquinoline‐4‐carboxylic acids analogous to antimalarial and antileishmanial natural products was developed __via__ the Döbner reaction employing microwave irradiation (MW). The products were obtained in moderate yields in 0.5‐3 minu
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.