Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60515
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dc.contributor.authorKurapati, Chidvilas-
dc.contributor.authorMuthukrishnan, M-
dc.contributor.authorSingh, Om V-
dc.contributor.authorGundla, Rambabu-
dc.date.accessioned2022-09-20T10:23:54Z-
dc.date.available2022-09-20T10:23:54Z-
dc.date.issued2022-09-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60515-
dc.description923-927en_US
dc.description.abstractA practical and effective approach towards the synthesis of 3-hetroaryl-4H-chromen-4-ones by the oxidative rearrangement of the respective 2-hetroaryl chroman-4-ones using thallium(III) p-tosylate is described. The oxidative rearrangement of α and β-naphthyl and thiophene behave like aryl groups. However, pyridyl groups give only the dehydrogenated product.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.61(09) [Sep 2022]en_US
dc.subjectOxidative rearrangementsen_US
dc.subjectthallium(III) p-tosylateen_US
dc.subjectdehydrogenationen_US
dc.subjectthallium(III) acetateen_US
dc.subject2- and 3-(β-naphthyl) chromonesen_US
dc.subject2- and 3-(2-theinyl)chromonesen_US
dc.subject2- and 3-(3-theinyl)chromonesen_US
dc.subject2-(3-pyridyl)chromonesen_US
dc.subject2-(4-pyridyl)chromonesen_US
dc.titleThallium(III) p-tosylate (TTS) mediated oxidative rearrangement of 2-naphthyl and 2-heteroarylchromanonesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i9.66341en_US
Appears in Collections:IJC Vol.61(09) [Sep 2022]

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