Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2321
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dc.contributor.authorMarkad, D.-
dc.contributor.authorMandal, S.K.-
dc.date.accessioned2020-11-27T06:51:29Z-
dc.date.available2020-11-27T06:51:29Z-
dc.date.issued2019-
dc.identifier.citationEuropean Journal of Organic Chemistry, 2019(4), pp. 705-714.en_US
dc.identifier.otherhttps://doi.org/10.1002/ejoc.201801292-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201801292-
dc.identifier.urihttp://hdl.handle.net/123456789/2321-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractA concise cascade strategy for the synthesis of 6H‐chromeno[4,3‐b]quinolin‐6‐ones was developed from 4‐hydroxycoumarins and arylhydrazine hydrochlorides in DMSO. The synthetic strategy relies on dual role of ammonium acetate in generating 4‐aminophenyl coumarin from arylhydrazine via aryl radical formation, and Csp2‐H formylation of coumarin using DMSO as a methine source. The strategy is scalable, and an array of arylhydrazine hydrochlorides delivered chromene‐fused quinolinones in good to excellent yields.en_US
dc.language.isoenen_US
dc.publisherWILEY‐VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.subjectNitrogen heterocyclesen_US
dc.subjectDomino reactionsen_US
dc.subjectCoumarinen_US
dc.titleNH4OAc‐Promoted Cascade Approach towards Aberrant Synthesis of Chromene‐Fused Quinolinonesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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