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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1424
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dc.contributor.authorKumar, V.N.-
dc.contributor.authorThirupathi Reddy, Y.-
dc.contributor.authorNarasimhareddy, P.-
dc.contributor.authorRajitha, B.-
dc.contributor.authorDe Clercq, E.-
dc.date.accessioned2024-11-11T10:45:03Z-
dc.date.available2024-11-11T10:45:03Z-
dc.date.issued2007-
dc.identifier.citation10.3998/ark.5550190.0007.f22en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1424-
dc.descriptionNITWen_US
dc.description.abstractSynthesis of meso-tetrakis (2, 10-dioxo-2H, 10H-pyrano[2,3-f] chromene-9-yl) porphyrins are synthesized directly by reaction of pyrrole with substituted 4-methyl-2,10-dioxo-2H, 10Hpyrano[2,3-f]chromene-9-carbaldehydes in dichloromethane / acid media. The aldehyde’s molar ratio was controlled to optimize the synthesis and purification of the desired porphyrins. This new series of porphyrins was characterized by TLC, Mass Spectrometry (FAB mass), 1 H NMR, UV and IRen_US
dc.language.isoenen_US
dc.publisherArkivocen_US
dc.subjectPorphyrins,en_US
dc.subjectChromene,en_US
dc.subjectTFAen_US
dc.titleSynthesis and biological activity of meso-tetrakis (2,10-dioxo-2H, 10H-pyrano [2,3-f] chromene-9-yl) porphyrinsen_US
dc.typeArticleen_US
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