Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/4555
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dc.contributor.authorBabu, S A-
dc.contributor.authorVarsha, P V-
dc.contributor.authorPoulose, S-
dc.contributor.authorVarughese, S-
dc.contributor.authorJohn, J-
dc.date.accessioned2023-11-04T08:23:52Z-
dc.date.available2023-11-04T08:23:52Z-
dc.date.issued2023-07-21-
dc.identifier.citationThe Journal of Organic Chemistry;88(14):10027-10039en_US
dc.identifier.urihttps://doi.org/10.1021/acs.joc.3c00849-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/4555-
dc.description.abstractWe have developed a direct method for the synthesis of polyring-fused imidazo[1,2-a]pyridines via a coppercatalyzed annulation of electrophilic benzannulated heterocycles with 2-aminopyridine and 2-aminoquinoline. From 3-nitroindoles and 2-aminopyridine, we could synthesize tetracenes, viz., indolefused imidazo[1,2-a]pyridines, and by starting from 2-aminoquinoline, we could generate pentacenes, viz., indolo-imidazo[1,2- a]quinolines. In addition, we could also extend the methodology toward the synthesis of benzothieno-imidazo[1,2-a]pyridines starting from 3-nitrobenzothiophene. Furthermore, the basic photophysical properties of these synthesized heteroacenes were evaluated.en_US
dc.language.isoenen_US
dc.publisherACS Publicationsen_US
dc.subjectBenzannulated Heterocyclesen_US
dc.subject2-Aminopyridine and 2-Aminoquinolineen_US
dc.titleCopper-Catalyzed Annulation of Electrophilic Benzannulated Heterocycles with 2-Aminopyridine and 2-Aminoquinoline: Direct Access toward Polyring-Fused Imidazo[1,2-a]pyridinesen_US
dc.typeArticleen_US
Appears in Collections:2023



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