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dc.contributor.authorAmaravathi, M.-
dc.contributor.authorBabu, M.M.-
dc.contributor.authorChandramouli, G.-
dc.date.accessioned2024-11-11T09:14:02Z-
dc.date.available2024-11-11T09:14:02Z-
dc.date.issued2007-
dc.identifier.citation10.3998/ark.5550190.0008.116en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1414-
dc.descriptionNITWen_US
dc.description.abstractmeso-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 oCen_US
dc.language.isoenen_US
dc.publisherArkivocen_US
dc.subjectN-aryl acetamidesen_US
dc.subjectVilsmeier–Haack cyclizationen_US
dc.titleSynthesis of meso- tetrakis (2-chloroquinolin-3-yl) porphyrinsen_US
dc.typeArticleen_US
Appears in Collections:Chemistry

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