Piperidine mediated synthesis of n-heterocyclic chalcones and their antibacterial activity
✍ Scribed by P. Venkatesan; S. Sumathi
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 80 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.268
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
magnified image
The chalcones 1‐(2′‐hydroxy‐aryl)‐3‐(1‐indol‐3‐yl)‐prop‐2‐en‐1‐one (3) and 1‐(2′‐hydroxy‐aryl)‐3‐(2‐chloroquinolin‐3‐yl)‐prop‐2‐en‐1‐one (6) were synthesised by piperidine mediated condensation of an ethanolic solution of an o‐hydroxyacetophenone (1) with corresponding heteroaryl‐3‐carboxaldehyde. The structures have been established on the basis of elemental (C, H, N) analysis, UV, IR, ^1^H NMR spectral data. The compounds 3 and 6 were screened for antimicrobial activities against a variety of bacterial agents. J. Heterocyclic Chem., 2010.
📜 SIMILAR VOLUMES
## Abstract A series of new thiazolyl chalcones, 1‐[2‐amino‐4‐methyl‐1, 3‐thiazol‐5‐yl]‐3‐aryl‐prop‐2‐en‐1‐one were prepared by piperidine mediated Claisen‐Schmidt condensation of thiazolyl ketone with substituted aromatic aldehyde. These chalcones on cyclization gave 2‐amino‐6‐(2‐amino‐4‐methyl‐1,
## Abstract For Abstract see ChemInform Abstract in Full Text.