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http://hdl.handle.net/123456789/2321
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DC Field | Value | Language |
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dc.contributor.author | Markad, D. | - |
dc.contributor.author | Mandal, S.K. | - |
dc.date.accessioned | 2020-11-27T06:51:29Z | - |
dc.date.available | 2020-11-27T06:51:29Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | European Journal of Organic Chemistry, 2019(4), pp. 705-714. | en_US |
dc.identifier.other | https://doi.org/10.1002/ejoc.201801292 | - |
dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201801292 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2321 | - |
dc.description | Only IISERM authors are available in the record. | - |
dc.description.abstract | A 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.iso | en | en_US |
dc.publisher | WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim | en_US |
dc.subject | Nitrogen heterocycles | en_US |
dc.subject | Domino reactions | en_US |
dc.subject | Coumarin | en_US |
dc.title | NH4OAc‐Promoted Cascade Approach towards Aberrant Synthesis of Chromene‐Fused Quinolinones | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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Need to add pdf.odt | 8.63 kB | OpenDocument Text | View/Open |
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