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http://localhost:8080/xmlui/handle/123456789/1414| Title: | Synthesis of meso- tetrakis (2-chloroquinolin-3-yl) porphyrins |
| Authors: | Amaravathi, M. Babu, M.M. Chandramouli, G. |
| Keywords: | N-aryl acetamides Vilsmeier–Haack cyclization |
| Issue Date: | 2007 |
| Publisher: | Arkivoc |
| Citation: | 10.3998/ark.5550190.0008.116 |
| Abstract: | meso-Tetrakis (-2-chloroquinolin-3-yl) porphyrins were synthesized from 2-chloroquinoline-3carboxaldehydes and pyrrole in 1:1 ratio in propionic acid at 140 oC for 4 hours. Different substituted 2-chloroquinoline-3-carboxaldehydes were synthesized from corresponding N-aryl acetamides by Vilsmeier–Haack cyclization. The aldehydes were obtained in better yields, when acetamides, dimethyl formamide and POCl3 were taken in 1:3: 7 molar ratios at 70-75 oC |
| Description: | NITW |
| URI: | http://localhost:8080/xmlui/handle/123456789/1414 |
| Appears in Collections: | Chemistry |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Synthesis of meso- tetrakis (2-chloroquinolin-3-yl) porphyrins.pdf | 208.12 kB | Adobe PDF | View/Open |
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