Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/1414Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Amaravathi, M. | - |
| dc.contributor.author | Babu, M.M. | - |
| dc.contributor.author | Chandramouli, G. | - |
| dc.date.accessioned | 2024-11-11T09:14:02Z | - |
| dc.date.available | 2024-11-11T09:14:02Z | - |
| dc.date.issued | 2007 | - |
| dc.identifier.citation | 10.3998/ark.5550190.0008.116 | en_US |
| dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/1414 | - |
| dc.description | NITW | en_US |
| dc.description.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 | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Arkivoc | en_US |
| dc.subject | N-aryl acetamides | en_US |
| dc.subject | Vilsmeier–Haack cyclization | en_US |
| dc.title | Synthesis of meso- tetrakis (2-chloroquinolin-3-yl) porphyrins | en_US |
| dc.type | Article | en_US |
| 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 |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.