Facile Synthesis of 11-aryl-6H-isoindolo [2,1-a]indol-6-ones via Hypervalent Iodine (III)-Promoted Cascade Cyclization

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dc.contributor.author Dev, Kapil
dc.contributor.author Maurya, Rakesh
dc.date.accessioned 2015-03-20T04:57:47Z
dc.date.available 2015-03-20T04:57:47Z
dc.date.issued 2015
dc.identifier.citation RSC Advances. 2015, 5, 13102-13106 en
dc.identifier.uri http://hdl.handle.net/123456789/1429
dc.description.abstract An efficient method was developed for the synthesis of tetracyclic fused indoleandisoindoline ring system, under metal-free conditions. The hypervalent iodine PIDA-mediated regioselective as well as chemoselective intramolecular cascade oxidative cyclization of 2-(1-arylethynyl)benzamides afforded 11-aryl-6H-isoindolo [2,1-a] indol-6-ones at room temperature in good to excellent yields. en
dc.format.extent 245624 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CSIR-CDRI Communication No. 8894 en
dc.subject Tetracyclic en
dc.subject Hypervalent Iodine en
dc.title Facile Synthesis of 11-aryl-6H-isoindolo [2,1-a]indol-6-ones via Hypervalent Iodine (III)-Promoted Cascade Cyclization en
dc.type Article en


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